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 25201–25220 of 27,462 recalls
Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR VACCESS¿ PTA Balloon Dilatation Catheters Recalled...
The Issue: Bard Peripheral Vascular (BPV) has confirmed that some product code/lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Elekta digital accelerators with electrons and beam modulator Recalled...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S3 ActiveTrack Excimer System (STAR S3) Mfg by AMO Manufacturing USA...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure Nephrostomy Balloon Catheter. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StarDental Classique(TM) Diamond Dental Bur. Used for specific applications...
The Issue: Recall was initiated because a manufacturing issue was found that prevented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...
The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 IR Excimer System (STAR S4 IR) Mfg by AMO Manufacturing USA Recalled...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.