Recalls affecting Vermont

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

Recall #:

89486

Lot/product code:

All Lots within Expiry Catalog No: 364902 UDI: (01)50382903649025 Catalog Number: 36490200 UDI:(01)60382903649022

Recalling firm:

Becton Dickinson & Company

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89619

Lot/product code:

Lot number 110221A1 UDI Number (01)00889024304222 (17)231103(10)110221A1

Recalling firm:

Orthosoft, Inc. dba Zimmer CAS

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89327

Lot/product code:

All lot numbers within expiry

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

89416

Lot/product code:

Product Number MDRGN2F; Lots: 1) B1402A (Expiration 2022/Oct05) 2) B1315A (Expiration 2022/Aug06) 3) B1211 (Expiration 2022/May24) 4) B1161A (Expiration 2022/Apr19 5) B0361 (Expiration 2021/Aug31) 6) B0164B (Expiration 2021/Apr16)

Recalling firm:

Remel Inc

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

Recall #:

89389

Lot/product code:

Lot/Serial # RM2005000001-RM21004005000 (May 2020 through April 2021 manufacture dates)

Recalling firm:

Compass Health Brands (Corporate Office)

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

Recall #:

89522

Lot/product code:

GTIN: 10888857261204; Lot Numbers: JUJF KFMV KUPG KYYU MDRB NDMK NDMX NXJK

Recalling firm:

K2M, Inc

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

Recall #:

89539

Lot/product code:

Part Number: I-114(S) Lot Numbers: All Lots due to not having an authorized Emergency Use Authorization (EUA)

Recalling firm:

Lusys Laboratories, Inc.

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

Recall #:

89522

Lot/product code:

GTIN: 10888857261211; Lot Numbers: HCBN HCBP JUJJ KFMX KUPH KYYV MDPF NAKJ NDGT PCCN

Recalling firm:

K2M, Inc

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

Recall #:

89539

Lot/product code:

Part Number: I-111 Lot Numbers: All Lots due to not having an authorized Emergency Use Authorization (EUA)

Recalling firm:

Lusys Laboratories, Inc.

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

Recall #:

89539

Lot/product code:

Part Number: I-114(N) Lot Numbers: All Lots due to not having an authorized Emergency Use Authorization (EUA)

Recalling firm:

Lusys Laboratories, Inc.

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

Recall #:

89524

Lot/product code:

All instrument serial numbers running running software versions 11.5, 11.5.1 and 11.5.2. with ONH Angiography 4.5x4.5mm Scan

Recalling firm:

Carl Zeiss Meditec, Inc.

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

Recall #:

D-0387-2022

Lot/product code:

Lot #: 32451 Exp. 03/2022; 32532 Exp. 04/2022; 32552 Exp. 05/2022; 32701 32733 Exp. 10/2022; 32855 Exp. 02/2023; 32872 Exp. 03/2023.

Recalling firm:

Mayne Pharma Inc

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

Recall #:

89592

Lot/product code:

Lot Numbers: 89648801 89648802 89648803 89648804 89648805 GTIN: 04546540608475 ****UPDATE 3/17/22: Lot Number: 89648802 UDI: " (01)04546540608475(17)261020(10)89648802 Removed from scope of Recall: 89648801 89648803 89648804 89648805

Recalling firm:

Howmedica Osteonics Corp.

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

Recall #:

89592

Lot/product code:

Lot Number: 89546202 GTIN: (01)04546540608536(17)261020(10)89546202

Recalling firm:

Howmedica Osteonics Corp.

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

Recall #:

89515

Lot/product code:

All serial numbers of 1688 CCU, UDI: 07613327420081, with Software Revisions: 3.0.6, 4.0.13, and 4.0.18

Recalling firm:

Stryker Corporation