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Becton Dickinson & Company recalls BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Recalled November 6, 2019 · FDA recall Z-0252-2020 · Becton Dickinson &
Hazard
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage. · FDA Class II
Units
2,624,160 (2,169,703 US; 454,457 OUS)
Sold at
Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan.
Description
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
Product
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →