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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 25761–25780 of 27,462 recalls
Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...
The Issue: The bed frame adapter assemblies may have a weak weld where the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...
The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...
The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...
The Issue: Out of specification result - stability test failure of free available...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...
The Issue: Philips was notified of a problem using the IntelliSpace Portal with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....
The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...
The Issue: Multiple incidents of low-reacting assay plates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer NexPosure Recalled by Zimmer, Inc. Due to Possibility that the inner...
The Issue: Possibility that the inner pouch may be compromised. The product is packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...
The Issue: Orthodontic brackets distributed was incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number Recalled...
The Issue: Increased risk of failure at the driver tip during screw insertion or removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.