Bedford Pharmacy Recalls P-P-P Injection Due to Sterility Concerns
Bedford Pharmacy is recalling P-P-P (COBAL) 30-4-40/mL Injection vials because there is a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.
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. According to the rubric, FDA Class II recalls with potential for serious injury (such as sterility issues in injections) are categorized as Severe.
Plain-English summary
Bedford Pharmacy is recalling one vial of P-P-P (COBAL) 30-4-40/mL Injection. The recall is being conducted because there is a lack of assurance of sterility for the product. The specific lot number is 09082015@4, and the expiration date is 10/23/2015.
The affected product was distributed in New Hampshire and Massachusetts. The recall is classified as Class II by the U.S. Food and Drug Administration.
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm, Bedford Pharmacy, for further instructions.
The recalled product
- Product
- P-P-P (COBAL) 30-4-40/mL, Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919
- Manufacturer
- Bedford Pharmacy
- Category
- Drug — Injection
- Hazard
- Affected units
- 1
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 (2)
- Lot #: 09082015@4
- Exp 10/23/2015
Distribution
Part of a larger recall action
This product is one of 13 recalled by Bedford 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.
See all 13 products in this recall →Related recalls
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- SevereBedford Pharmacy Recalls P-P (COBAL) Injection Due to Sterility Concerns
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