Class II · Moderate risk Terminated
Meperidine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Reason Lack of sterility assurance.
Is Meperidine recalled?
4 FDA recalls mention Meperidine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Meperidine.
Class II · Moderate risk Terminated
Meperidine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Class III · Low risk Terminated
Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake…
Reason Labeling; Missing label; ampoules are missing the immediate container label
Class II · Moderate risk Terminated
Meperidine 100mg/ml MDV, 5ml 90 day expiration,
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
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