B&B Pharmacy Recalls PAPA/PHENTO Injection Due to Sterility Concerns
Pacific Healthcare, Inc dba B&B Pharmacy is recalling PAPA/PHENTO Injection vials because FDA inspections identified GMP violations that may affect sterility.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a lack of assurance of sterility in an injectable medication, which poses a significant risk of serious injury or death if contaminated.
Plain-English summary
Pacific Healthcare, Inc dba B&B Pharmacy is recalling PAPA/PHENTO (30mg/1mg/ml) Injection, 5 mL and 10 mL vials. The recall was initiated because FDA inspections identified Good Manufacturing Practice (GMP) violations that potentially impact the product's quality and sterility.
The affected products are prescription (Rx) vials distributed in California and New Jersey. Specific lot codes and expiration dates are listed in the recall documentation, including 5 mL vials expiring in January 2016 and 10 mL vials expiring in November 2015, January 2016, and February 2016.
Consumers and healthcare providers should stop using the recalled product and contact their pharmacist or the recalling firm for instructions on return or replacement.
The recalled product
- Product
- PAPA/PHENTO (30mg/1mg/ml) Injection, 5 mL and 10 mL vials, Rx, B & B Health Mart Pharmacy, Bellflower, CA
- Manufacturer
- Pacific Healthcare, Inc dba B&B Pharmacy
- Category
- Drug — Injectable Medication
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (8)
- 5 ml --- 07212015@2
- exp 1/17/2016
- 10 ml --- 05062015@17
- exp 11/2/2015
- 07082015@10
- exp 1/4/2016
- 08312015@3
- exp 2/20/2016
Distribution
Part of a larger recall action
This product is one of 16 recalled by Pacific Healthcare, Inc dba B&B Pharmacy under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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