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. 2,448 recalls have been distributed to Wyoming in the last 12 months.
Showing 19761–19780 of 27,462 recalls
Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...
The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...
The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...
The Issue: Incorrect expiration date was listed on the label. Correct expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...
The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Assay: LDL Cholesterol Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.