US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 21, 2013 (13 years ago)

MERREM I.V. (meropenem for injection), 1 g meropenem equivalent, 30 mL vial, Rx only, Mfd…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Precipitate; potential for incomplete constitution upon addition of diluent.

What was recalled

MERREM I.V. (meropenem for injection), 1 g meropenem equivalent, 30 mL vial, Rx only, Mfd for: AstraZeneca Pharmaceuticals LP, Wilmington, DE by ACS Dobfar SpA Viale Addetta, Tribiano, Milano Italy NDC 0310 0321 30

Recalling firm
AstraZeneca Pharmaceuticals LP
Origin
DE, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-840-2013

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.

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