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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Pharmatech LLC

31 recall records in Supplements.

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31 recalls grouped by year

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2016

9 records

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

2015

2 records

Class IITerminated06/17/2015Recall F-2405-2015

Product description

Rugby Poly Vitamin Liquid, 50ml

Reason for recall

Packaging label does not match individual product labeling. Outside packaging may have incorrect Lot/Exp and product identity.

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Event ID: 70937
Code info: UPC: 05368-45080 Lot: 20701407
Product quantity: 59,930units
Distribution pattern: NY, IL, TX, UT, MN, AL, CO, CA, WA, VA, MA, AZ, GA, KY, HI, OH, NC, MI, FL, PA, MO, MS, VT, ND, IN, NH, NJ, OR, TN, OK, NE, WI, MO, CT, LA, SC, AR, PR
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type: Food
Recalling firm location: 4111 Sw 47th Ave, Suite 333, Davie, FL, United States
Recall initiation date: 03/09/2015
Center classification date: 06/08/2015
Termination date: 07/05/2016

Class IITerminated06/17/2015Recall F-2406-2015

Product description

Rugby Poly Vitamin Liquid with Iron, 50 ml

Reason for recall

Packaging label does not match individual product labeling. Outside packaging may have incorrect Lot/Exp and product identity.

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Event ID: 70937
Code info: UPC: 05368-53080 Lot: 21021410
Product quantity: 52,554 units
Distribution pattern: NY, IL, TX, UT, MN, AL, CO, CA, WA, VA, MA, AZ, GA, KY, HI, OH, NC, MI, FL, PA, MO, MS, VT, ND, IN, NH, NJ, OR, TN, OK, NE, WI, MO, CT, LA, SC, AR, PR
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type: Food
Recalling firm location: 4111 Sw 47th Ave, Suite 333, Davie, FL, United States
Recall initiation date: 03/09/2015
Center classification date: 06/08/2015
Termination date: 07/05/2016