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FDA (Device enforcement)Recalled 2023-04-17class ii

DeRoyal Industries Inc: Sterile custom surgical procedure packs: (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital; (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital; (3) 89-10509.02,

Hazard

The custom procedure packs contain light handle covers that have been recalled by another firm.

Details from the source

Reason for recall: The custom procedure packs contain light handle covers that have been recalled by another firm. Distribution: US Nationwide distribution in the state of VA. Quantity: 1,391 cases (2,972 packs) Lot/code info: (1) 89-10507.02 - lot 58700464, exp 12/1/2024, GTIN pack-00749756362788, case-50749756362783; (2) 89-10508.02 - lot 58700430, exp 9/1/2026, GTIN pack-00749756362818, case-50749756362813; (3) 89-10509.02 - lot 58775010, exp 12/1/2024, GTIN pack-00749756362832, case-50749756362837; (4) 89-10517.04 - lot 58700579, exp 12/1/2024, GTIN pack-00749756363228, case-50749756363223; (5) 89-10526.04 - lot 58388765, exp 11/1/2024, GTIN pack-00749756363242, case-50749756363247; (6) 89-10530.04 - lot 58543121, exp 11/1/2024, GTIN pack-00749756364447, case-50749756364442; (7) 89-10532.04 - lot 58543905, exp 7/1/2024, GTIN pack-00749756363266, case-50749756363261; (8) 89-10534.02 - lots 58565821 and 58700561, exp 3/1/2024, GTIN pack-00749756363532, case-50749756363537; (9) 89-10544.03 - lot 58700000, exp 10/1/2024, GTIN pack-00749756366342, case-50749756366347; (10) 89-10545.02 - lot 58565830, exp 3/1/2024, GTIN pack-00749756363556, case-50749756363551; (11) 89-10552.02 - lot 58700667, 58700675, and 58724108, exp 12/1/2024, GTIN pack-00749756363549, case-50749756363544; (12) 89-10553.02 - lot 58544060, exp 11/1/2024, GTIN pack-00749756363624, case-50749756363629; (13) 89-10554.02 - lot 58544166, exp 12/1/2024, GTIN pack-00749756363440, case-50749756363445; (14) 89-10555.02 - lot 58589647 and 58724116, exp 12/1/2024, GTIN pack-00749756363648, case-50749756363643; (15) 89-10556.02 - lot 58589567, exp 12/1/2024, GTIN pack-00749756364287, case-50749756364282; (16) 89-10558.04 - lot 58542769, exp

UPC codes

00749756362788, 50749756362783, 00749756362818, 50749756362813, 00749756362832, 50749756362837, 00749756363228, 50749756363223, 00749756363242, 50749756363247, 00749756364447, 50749756364442, 00749756363266, 50749756363261, 00749756363532, 50749756363537, 00749756366342, 50749756366347, 00749756363556, 50749756363551, 00749756363549, 50749756363544, 00749756363624, 50749756363629, 00749756363440, 50749756363445, 00749756363648, 50749756363643, 00749756364287, 50749756364282, 00749756364430, 50749756364435, 00749756363778, 50749756363773, 00749756363723, 50749756363728, 00749756364140, 50749756364145, 00749756363761, 50749756363766

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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