Recalls affecting Louisiana

FDA has not published a risk classification for this recall yet.

Recall #:

97967

Lot/product code:

1. UDI-DI 848838018831, lots 305529, 311228, 316019, 320993 2. UDI-DI 848838091353, lot 317287

Recalling firm:

Remel, Inc

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

D-0179-2026

Lot/product code:

Lot#: 71409, Expires: 02/28/2027; 71861, Expires: 08/31/2027.

Recalling firm:

Medical Products Laboratories, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

97976

Lot/product code:

Product Code Lot # UDI-DI (GTIN): CT5500T ALL LOT NUMBERS LESS THAN OR EQUAL TO 22GASN045 CS- 50885380172371 EA- 20885380172370; CT5502T ALL LOT NUMBERS LESS THAN OR EQUAL TO 22GASN044 CS 50885380172395 EA - 20885380172394; CT5503T ALL LOT NUMBERS LESS THAN OR EQUAL TO 22GASN036 CS 50885380172418 EA - 20885380172417; CT5504T ALL LOT NUMBERS LESS THAN OR EQUAL TO 22EASN004 CS- 50885380172432 EA- 20885380172431; CT5505T ALL LOT NUMBERS LESS THAN OR EQUAL TO 22GASN043 CS- 50885380172456 EA- 20885380172455; DP5001GT ALL LOT NUMBERS LESS THAN OR EQUAL TO 22GASN033 CS- 50885380173989 EA-20885380173988; DP5002GT ALL LOT NUMBERS LESS THAN OR EQUAL TO 22EASN020 CS- 50885380173996 EA-20885380173995; DP5003GT ALL LOT NUMBERS LESS THAN OR EQUAL TO 22GASN020 CS- 50885380173972 EA-20885380173971; DP5004GT ALL LOT NUMBERS LESS THAN OR EQUAL TO 22BASN087 CS- 50885380174009 EA-20885380174008; CT5500TS 21KAS095 CS- 50885380172388 EA-20885380172387; CT5502TS 21KAS059 CS- 50885380172401 EA-10885380172403; CT5503TS 21KAS106, 21LAS004, 21LAS017 CS- 50885380172425 EA-10885380172427; CT5504TS 21KAS064, 21KAS072, 21KAS109 CS- 50885380172449 EA-10885380172441; CT5505TS 21KAS019, 21KAS031 CS- 50885380172463 EA-10885380172465;

Recalling firm:

Cardinal Health 200, LLC

FDA has not published a risk classification for this recall yet.

Recall #:

98060

Lot/product code:

Kit Code: LLOF1000-17; UDI : 10809160460726, Lot No : 1651709

Recalling firm:

AVID Medical, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98060

Lot/product code:

Kit Code: JACK097-08; UDI : 10809160462829; Lot No: 1654185.

Recalling firm:

AVID Medical, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98060

Lot/product code:

Kit Code: LLOG1000-15; UDI: 10809160432679; Lot No: 1632138 & 1648393.

Recalling firm:

AVID Medical, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A2660T; UDI: 04042761004183; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. WA22017A; UDI: 04042761051514; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98056

Lot/product code:

Lot 19019 UDI-DI 10193489131703

Recalling firm:

Medline Industries, LP

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22043A; UDI: 04042761021005; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22042T; UDI: 04042761020992; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A2660; UDI: 04042761004176; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A4741; UDI: 04042761006514; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22042A; UDI: 04042761020985; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A2642; UDI: 04042761004084; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A2666T; UDI: 04042761004251; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. Model No. A22041A; UDI: 04042761020961; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A42011A; UDI: 04042761023658; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22043T; UDI: 04042761021012; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A37004A; UDI: 04042761023092; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22041T; UDI: 04042761020978; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A2666; UDI: 04042761004244; All Lots

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22040T; UDI: 04042761029360; All Lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model: A22014A (UDI: 04042761020893) and A22014T (UDI: 04042761020909). All lots.

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

98288

Lot/product code:

Model No. A22040A; UDI: 04042761029339; All Lots.

Recalling firm:

Olympus Corporation of the Americas