Class II · Moderate risk
Meperidine HCl in 0.9% Sodium Chloride in all strengths
Lack of sterility assurance.
Is Meperidine recalled?
Not under an active recall.
Meperidine was recalled 4 times in the past — all now closed. Most recent: Dec 27, 2017.
Most common reason: Labeling / mix-up (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Meperidine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Meperidine recalls on record
none so far in 2026; 4 on record, newest first
Class II · Moderate risk
Meperidine HCl all strengths
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Class III · Low risk
Demerol
Labeling; Missing label; ampoules are missing the immediate container label
Class II · Moderate risk
Meperidine 100mg/ml MDV
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
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