Liberty Drug Recalls Doxycycline IV Bags Due to Sterility Concerns
Liberty Drug & Surgical is recalling 30 bags of Doxycycline/0.9% NaCl IV due to process deficiencies that could have compromised 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 involves a risk of serious health consequences (loss of sterility in injectable products), which aligns with the 'Severe' criteria for significant injury risk or Class II classifications with potential for serious harm.
Plain-English summary
Liberty Drug & Surgical is recalling 30 bags of Doxycycline/0.9% NaCl 300 mg/500 mL IV, prescription only. The recall is due to process deficiencies observed in sterile ophthalmic and injectable products that could have compromised the sterility of the product.
The affected lots are 05142015@20 (Exp 07/06/15) and 05282015@15 (Exp 07/06/15). The product was distributed to physicians, medical facilities, and prescription-specific patients in New Jersey and New York.
Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Doxycycline/0.9% NaCl 300 mg/500 mL IV, 500 mL bag, Rx only, Liberty Drug Compound Center, 195 Main St., PO Box 267, Chatham, NJ 07928.
- Manufacturer
- Liberty Drug & Surgical
- Category
- Drug — Injectable
- Hazard
- Affected units
- 30
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 (3)
- Lot #: 05142015@20
- Exp 07/06/15
- 05282015@15
Distribution
Part of a larger recall action
This product is one of 25 recalled by Liberty Drug & Surgical 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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