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FDA (Device enforcement)Recalled 2023-04-21class ii

MEDLINE INDUSTRIES, LP - Northfield: Procedure packs: (1) Medline Sterile Arthroscopy Pack, REF: DYNJ64242B; (2) Medline Sterile Shoulder Pack, REF: DYNJ64250A; and (3) Medline Sterile Upper Extremity

Hazard

The kits were damaged by water.

Details from the source

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.

UPC codes

10193489956405, 10193489429817, 10193489968453

Source

Official record: FDA (Device enforcement)

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

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