Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

Event 78978: Why was this Pharmatech LLC product recalled?

Presence of yeast and potential contamination with B. cepacia.

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For this brand

Pharmatech LLC

42 recall records on file.

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Search within this brand by product, lot, or recall number.

42 recalls grouped by year

2016

20 records

Class IITerminated11/02/2016Recall F-0257-2017

Product description

D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005368400806; Lot No. 20691509, Exp. Date11/2017; Lot No. 20691601, Exp. Date 01/2018; Lot No. 20691602, Exp. Date 02/2018; Lot No. 20691604, Exp. Date 05/2018.
Product quantity: 229,464 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0258-2017

Product description

Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005362790590; Lot No. 20471516, 20471517, 20471518, 20471519, & 20471520, Exp. Date 11/2017; Lot No. 20471521, Exp. Date 12/2017; Lot No. 20471601, Exp. Date 01/2018; Lot No. 20471608, Exp. Date 04/2018; Lot No. 20471610 & 20471613, Exp. Date 05/2018; Lot No. 20471614, Exp. Date 06/2018.
Product quantity: 129,268 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0259-2017

Product description

Ferrous Sulfate Liquid, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005360650858; Lot No. 22461511 & 22461512, Exp. Date 10/2017; Lot No. 22461513 & 22461514, Exp. Date 11/2017; Lot No. 22461515 & 22461516, Exp. Date 12/2017; Lot No. 22461601 & 22461602, Exp. Date 02/2018; Lot No. 22461603 & 22461604, Exp. Date 04/2018; Lot No. 22461605 & 22461606, Exp. Date 05/2018.
Product quantity: 75,972 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0260-2017

Product description

Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005360710804; Lot No. 20901507, Exp. Date 07/2017; Lot No. 20901507, Exp. Date 11/2017; Lot No. 20901603, Exp. Date 05/2018
Product quantity: 99,024 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0261-2017

Product description

Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005360710801; Lot No. 21021510, Exp. Date 07/2017; Lot No. 21021601, Exp. Date 01/2018; Lot No. 21021602, Exp. Date 02/2018; Lot No. 21021604, Exp. Date 05/2016.
Product quantity: 201,784 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0262-2017

Product description

Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005368450801; Lot No. 20701511, Exp. Date 09/2018; Lot No. 20701514, Exp. Date 12/2017; Lot No. 20701605, Exp. Date 05/2018; Lot No. 20701606, Exp. Date 06/2018.
Product quantity: 188,640 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0263-2017

Product description

Tri-Vitamin, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005368501800; Lot No. 20731506, Exp. Date 08/2017; Lot No. 20731603, Exp. Date 02/2018; Lot No. 20731604, Exp. Date 06/2018.
Product quantity: 105,456 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0264-2017

Product description

Liquid Vitamin C, 4 oz./118 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 005360160975; Lot No. 20331510 & 20331511, Exp. Date 12/2017; Lot No. 20331601 & 20331602, Exp. Date 03/2018.
Product quantity: 48,024 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0265-2017

Product description

CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 0904-5023-09; Lot No. 20471602, Exp. Date 01/2018; Lot No. 20471603 & 20471604, Exp. Date 02/2018; Lot No. 20471605 & 20171606, Exp. Date 03/2018; Lot No. 20471607, Exp. Date 04/2018; Lot No. 20471609, 20471611& 20471612, Exp. Date 05/2018.
Product quantity: 110,136 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0266-2017

Product description

Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 0904-5099-50; Lot No. 20701509 & 20701511, Exp. Date 09/2017; Lot No. 20701513, Exp. Date 12/2017; Lot No. 20701601, Exp. Date 02/2018; Lot No. 20701602 & 20701603, Exp. Date 04/2018; Lot No. 20701606, Exp. Date 06/2016.
Product quantity: 42,984 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0267-2017

Product description

Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 0904-5100-50; Lot No. 21021510, Exp. Date 07/2017; Lot No. 21021601, Exp. Date 01/2018; Lot No. 21021602, Exp. Date 02/2016; Lot No. 21021603, Exp. Date 04/2018; Lot No. 21021604, Exp. Date 05/2018.
Product quantity: 47,525 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0268-2017

Product description

D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 0904-6273-50; Lot No. 20691509, Exp. Date 11/2017; Lot No. 20691510, Exp. Date 12/2017; Lot No. 206916603, Exp. Date 03/2018; Lot No. 20691605, Exp. Date 04/2018.
Product quantity: 90,504 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0269-2017

Product description

Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 0904-6060-50; Lot No. 20901509 & 20901510, Exp. Date 11/2017; Lot No. 20901601, Exp. Date 02/2018; Lot No. 20901602, Exp. Date 03/2018; Lot No. 20901603, Exp. Date 05/2018.
Product quantity: 31,224 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0270-2017

Product description

Tri-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 0904-6274-50; Lot No. 20731506, Exp. Date 08/20107; Lot No. 20731507, Exp. Date 11/2017; Lot No. 20731604 & 20731605, Exp. Date 06/2018.
Product quantity: 23,736 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0271-2017

Product description

Pedia Tri-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 76518-020-50, Lot No. 20731506, Exp. Date 08/2017; Lot No. 20731508, Exp. Date 11/2017.
Product quantity: 8,712 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0272-2017

Product description

Pedia Tri-Vite Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 76518-040-50, Lot No. 21021511, Exp. Date 11/2017.
Product quantity: 6,024 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0273-2017

Product description

Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 76518-030-50; Lot No. 20701512, Exp. Date 11/2017.
Product quantity: 6,600 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0274-2017

Product description

Pedia D-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: NDC No. 76518-050-50; Lot No. 20691509, Exp. Date 11/2017
Product quantity: 5,040 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0275-2017

Product description

Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: Lot No. 30161601, Exp. Date 01/2018; Lot No. 30161602 & 30161603.
Product quantity: 62,228 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024

Class IITerminated11/02/2016Recall F-0276-2017

Product description

CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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Event ID: 75272
Code info: UPC No. 632687615989; Lot No. 30661601, Exp. Date 05/2018.
Product quantity: 1,990 bottles
Distribution pattern: FL, MI, MS, and OH.
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Letter
Product type: Food
Recalling firm location: 4131 SW 47th Ave Ste 1403, Davie, FL, United States
Recall initiation date: 08/08/2016
Center classification date: 10/25/2016
Termination date: 09/23/2024