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. 1,020 recalls have been distributed to Wyoming in the last 12 months.
Showing 15321–15340 of 48,219 recalls
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...
The Issue: CGMP Deviaitons
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Moisture Limits: Out of specification for water content
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...
The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...
The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...
The Issue: Aftermarket front bezel components were installed during service/repair, not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received...
The Issue: Firm received increased number of reports that VenaSeal dispensing systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BPB medica OSTEOBELL EXPLANT NEEDLE FOR BONE MARROW EXPLANT Recalled by...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normand Remisol Advance Data Manager is a software device that Recalled by...
The Issue: Instructions For Use for software versions 1.5 to 1.9 did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BPB medica CEMIX Recalled by BIOPSYBELL S.R.L. Due to Products labeled as...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) Recalled by BIOPSYBELL...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8G DIRECT WORKING CANNULA BEVEL TIP Recalled by BIOPSYBELL S.R.L. Due to...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP Recalled...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE CEMENT DELIVERY CANNULA Recalled by BIOPSYBELL S.R.L. Due to...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEMIX - CEMENT MIXING SYSTEM Recalled by BIOPSYBELL S.R.L. Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.