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. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24621–24640 of 27,462 recalls
Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...
The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570 with Urethane armrests Recalled by Winco Mfg.,...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: chromID Salmonella Agar Recalled by bioMerieux, Inc. Due to Potential...
The Issue: Complaints for Salmonella strains growing on this medium producing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Bone Innovations (SBi) rHead Radial Stem Recalled by Small Bone...
The Issue: The recall was initiated due to an increased risk of implants breaching the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DROP-ARM CONVALESCENT RECLINER 5271/5281 with One-touch release for...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XL CONVALESCENT RECLINER 5291/529S with Padded armrests with guard Recalled...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONVALESCENT RECLINER 5251/5261 Recalled by Winco Mfg., LLC Due to A...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: AVEA¿ Ventilator. All Models. The affected devices are...
The Issue: CareFusion has identified a potential risk associated with AVEA¿ ventilators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cranial Access (CRAK) Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra is recalling certain lots of Cranial Access Kit due to a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Siemens Rad Fluoro Uro Systems) Ysio Recalled by Siemens Medical Solutions...
The Issue: A potential malfunction and hazard to patients exists when using the Ysio,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2400 System Software V4.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1800 System Software V2.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia Recalled by...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1200 System Software: 1) V2.00 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1650 System Software: 1) V4.01 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: There are artifacts appearing on the Tracker images during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT¿ Femoral Stem (CPT 12/14 STEM SIZE 0 COCR Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.