Pharmatech LLC Recalls Recalls by year
A bar chart of the number of recalls naming this company by year.
Recalls by year
Year Recalls 2016 30 2018 21
Download CSV FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement. Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
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FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
View recall →
FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
View recall →
FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplem… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
View recall →
FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dieta… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
View recall →
FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
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FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary suppleme… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
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FDA Recall
🇺🇸 United StatesTerminated
Historical record Class II
Pharmatech LLC Product
Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL,… Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. Published
November 2, 2016 Distribution
FL, MI, MS, and OH.
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FDA Recall
Terminated
Historical record Class II
Senna Syrup (sennosides) 8.8 mg, 8 fl. oz. (237 mL) bottle, Distributed by: Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-6289-09. by Pharmatech LLC
Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia. Published
October 5, 2016 Distribution
Nationwide
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FDA Recall
Terminated
Historical record Class II
Senexon Liquid (sennosides) 8.8 mg, 8 fl oz. (237 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1000-59. by Pharmatech LLC
Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia. Published
October 5, 2016 Distribution
Nationwide
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FDA Recall
Terminated
Historical record Class II
Diocto Syrup (docusate sodium), 60 mg/15 mL, One Pint (473 mL) bottle, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1001-85. by Pharmatech LLC
Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia. Published
October 5, 2016 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Aller-Chlor (chlorpheniramine maleate) Syrup, USP, 2 mg in each 5 mL, 4 fl oz (120 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1025-47. by Pharmatech LLC
Reason
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia. Published
October 5, 2016 Distribution
Nationwide
View recall →
This page lists recalls that name Pharmatech LLC as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
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