Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,573 recalls have been distributed to Wyoming in the last 12 months.
Showing 2801–2820 of 27,462 recalls
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack...
The Issue: Certain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: intelliPATH Universal HRP Detection Kit Recalled by Biocare Medical, LLC Due...
The Issue: Kits containing the DAB chromogen buffer, intended for use in either manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System Recalled...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of...
The Issue: Potential challenge with intraoperative assembly of the external taper of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard PACEMAKER PACK - Medical convenience kits Model Number: MAMC223-08...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard D & C PACK-CKC - Medical convenience kits Model Number: BMGT003-02...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard CPT PEDS ADULT CH PACK - Medical convenience kits Recalled by AVID...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard OR ENDOVASCULAR TRAY - Medical convenience kits Model Number:...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.