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. 1,072 recalls have been distributed to Wyoming in the last 12 months.
Showing 7201–7220 of 48,219 recalls
Recalled Item: STERILE POVIDONE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVP SOLUTION SING STRL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The product description on the labeling includes the word "Sterile" or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Mode Stimulator Recalled by Liberty Medical Solutions, LLC Due to The...
The Issue: The instruction manuals that were included with the Multi-Mode Stimulators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura...
The Issue: Ceiling mounted L-arm contains a rotation cover that may potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion...
The Issue: Ceiling mounted L-arm contains a rotation cover that may potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- Recalled by Inpeco...
The Issue: Firmware of the Interface Module with Roche Cobas 8000 and Cobas PRO (CO8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...
The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4...
The Issue: Under certain circumstances, information from HL7 messages received by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump...
The Issue: In affected products, the tubing outer diameter may vary in size or the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trospium Chloride Extended-Release Capsules Recalled by Padagis US LLC Due...
The Issue: Failed Tablets/Capsules specifications; missing/broken/extra tablets within...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.