The kits were damaged by water.
Reason for recall: The kits were damaged by water. Distribution: Distribution was made to California. There was no foreign/government/military distribution. Quantity: 342 packs (114 packs/product) Lot/code info: (1) Arthroscopy Pack - Lot #22HMD098, Exp. 2024-04-30, UDI/DI (01)10193489956405; (2) Shoulder Pack -Lot #22JMA673, Exp. 2024-01-31, GTIN (01)10193489429817; and (3) Upper Extremity Pack - Lot #HMF900, Exp. 2024-01-31, UDI/DI (01)10193489968453.
10193489956405, 10193489429817, 10193489968453
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.