Reason for Recall
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Advertisement
Recall NumberZ-1496-2026ClassificationClass IIStatusOngoingCategorydeviceInitiated2026-01-27Reported2026-03-18DistributionUS Nationwide distribution in the states of California and Texas.Code InfoCatalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.