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. 2,466 recalls have been distributed to Wyoming in the last 12 months.
Showing 16341–16360 of 48,219 recalls
Recalled Item: Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK Recalled by...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: Recalled by...
The Issue: Revised Instruction Manual to the most accurate illustration for Mayfield...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph - Product Usage: intended to be a...
The Issue: The radio within the device can become disassociated with the wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levocetirizine Dihydrochloride Tablets Recalled by InvaTech Pharma...
The Issue: Failed Impurities/Degradation Specifications: One lot of Levocetirizine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA Due to Superpotent...
The Issue: Superpotent Drug: High out-of-specification assay results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Tablets Recalled by EYWA PHARMA INC Due to Presence of foreign...
The Issue: Presence of foreign tablet/capsule: A 1000 mg Levetiracetam Tablet was found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...
The Issue: The products subject to this recall may contain obvious, incorrect pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Slim Recalled by TissueTech, Inc. Due to Potential exposure of...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Plus Recalled by TissueTech, Inc. Due to Potential exposure of...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...
The Issue: Potential for no-flow and leaks under the twist clamp.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Recalled by TissueTech, Inc. Due to Potential exposure of product to...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended...
The Issue: Due to a potential software issue, the display may show the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to A...
The Issue: A software problem has been identified which could result in the CT Scanner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Mobile X-Ray System Recalled by Shimadzu Medical Systems Due to...
The Issue: There is a potential that the adjustable handle option on the X-Ray system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-ACT Actalyke Clotting Test Tubes that are used in the: Recalled by Helena...
The Issue: Due to complaints received associated with cracked/split test tube caps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citrasate Liquid Acid concentrate bottles Recalled by Fresenius Medical Care...
The Issue: The sodium and/or calcium levels in these concentrates were below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.