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. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14041–14060 of 27,462 recalls
Recalled Item: Implant Retrieval Instrument CC NP & Ext Hex WP 22 Recalled by Nobel Biocare...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Instrument CC RP & Tri Ch Hex WP Recalled by Nobel Biocare...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered RP 4.3x10 mm Single-Pat - Product Usage: The Recalled by Nobel...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Instrument Hex & Tri-Ch NP/RP 22mm - Product Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Kit - Product Usage: The kit itself does Recalled by Nobel...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abutment Screw Retrieval Instrument RP/WP/6.0 - Product Usage: The...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Instrument Tri Channel 6.0 22 mm - Product Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered RP 4.3x13 mm Single-Pat - Product Usage: The Recalled by Nobel...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gridlock Ankle Screw Driver Bit - Product Usage: Recalled by Trilliant...
The Issue: A screwdriver used to facilitate implant insertion and removal was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow Disposable Cartridge Recalled by Vyaire Medical Due to Testing has...
The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow Disposable Cartridge with IV Extension Set Recalled by Vyaire Medical...
The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Clinch II Auto Suture Grasper Recalled by COVIDIEN LLC Due to...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure kits include devices from the affected lots distributed OUS...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...
The Issue: 2.5 Truliant Fit Trays were mismarked as 3
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.