Class II · Moderate risk Terminated
Meropenem
Reason Lack of sterility assurance
MEROPENEM in NS
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
What was recalled
MEROPENEM in NS, Packaged as a) 1000MG in 250ML Homepumps, and b) 2GM in 100ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.
- Recalling firm
- Sentara Enterprises
- Origin
- VA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0611-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Meropenem recalls
See all
Class II · Moderate risk Terminated
Meropenem for Injection
Reason Lack of assurance of sterility: loss of container integrity.
Class II · Moderate risk Terminated
Meropenem 2 grams in 100 mL 0.9% NS bag
Reason Lack of Sterility Assurance
Class II · Moderate risk Terminated
Meropenem 1 g/NS 100 mL Minibag Plus
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Meropenem various strengths in normal saline bags
Reason Lack of sterility assurance.
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