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. 2,529 recalls have been distributed to Wyoming in the last 12 months.
Showing 10921–10940 of 27,462 recalls
Recalled Item: Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to...
The Issue: The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ULTRA Advanced Staining System (RUO-Research Use Only) Material...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Nephrostomy Stent Set Recalled by Cook Inc. Due to The indwell...
The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Neonatal Pigtail Nephrostomy Set Recalled by Cook Inc. Due to...
The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for...
The Issue: Brainlab Ultrasound Navigation Software does not support the modification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...
The Issue: Due to a potential manufacturing issue (cross contamination), composite is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope...
The Issue: The BF-Q180 bronchoscope is being recalled because it does not have a 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator Recalled by Greiner...
The Issue: Blood collection tubes experienced an issue with separation and clotting
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens epoc BGEM Test Card-In vitro diagnostic device for the Recalled by...
The Issue: Sporadically inconsistent discrepant (low bias) glucose results on card lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albumin Gen.2 Recalled by Roche Diagnostics Operations, Inc. Due to Roche...
The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant Complement C4 ver.2 Recalled by Roche Diagnostics Operations,...
The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol...
The Issue: Due to alkaline phosphatase (ALP) associated interference causing falsely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...
The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...
The Issue: Subsequent failure of catheters in the field and failed quality testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM HER-2/neu (H2n) assay Recalled by Siemens Healthcare...
The Issue: Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.