FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Calcionate Syrup 16 oz. UPC 00536-2770-85
- Reason
- Presence of yeast and potential contamination with B. cepacia.
- Published
- January 31, 2018
- Distribution
- MI
Pharmatech LLC
Recalls
A bar chart of the number of recalls naming this company by year.
| Year | Recalls |
|---|---|
| 2016 | 30 |
| 2018 | 21 |
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major Ferrous Drop Iron Supplement 50 mL UPC 00904-6060-50
- Reason
- Presence of yeast and potential contamination with B. cepacia.
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby FER Iron Liquid 50 mL UPC 00536-0710-80
- Reason
- Presence of yeast and potential contamination with B. cepacia.
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Ferrous Sulfate Elixir 473 mL UPC: 00536-0650-85
- Reason
- Presence of yeast and potential contamination with B. cepacia.
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-01…
- Reason
- Presence of yeast and potential contamination with B. cepacia.
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall Terminated Historical recordClass II
Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47, Manufactured by PharmaTech LLC, Davie FL
- Reason
- Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
- Published
- January 24, 2018
- Distribution
- MI
FDA Recall Terminated Historical recordClass II
Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59 ; ALSO LABELED AS Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09; Manufactured by PharmaTech LLC, Davie, FL
- Reason
- Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
- Published
- January 24, 2018
- Distribution
- MI
FDA Recall Terminated Historical recordClass II
Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1001-85, Manufactured by PharmaTech LLC, Davie, FL
- Reason
- Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
- Published
- January 24, 2018
- Distribution
- MI
FDA Recall Terminated Historical recordClass II
Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85, Manufactured by PharmaTech LLC, Davie, FL
- Reason
- Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
- Published
- January 24, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Pedia D-Vite Drops, 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.
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Pedia Tri-Vite Drops, 50 mL, OTC Non-Sterile. Dietary suppl…
- 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.
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Tri-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.
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. Read the full medical disclaimer.
