Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,069 recalls have been distributed to Iowa in the last 12 months.
Showing 14301–14320 of 28,127 recalls
Recalled Item: Drill Tapered WP 5x11.5 mm Single-Pat - Product Usage: Drills 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 Hex & Tri-Chi NP/RP 31mm - 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 NP 3.5x8 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: Dense Bone Drill 6.0 6x16 mm Single-Pat- Product Usage: The 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 NP 3.5x10 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: Abutment Screw Retrieval Instrument 3.0/NP - Product Usage: The instruments...
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: Screw Tap Tapered WP Single-Pat - Product Usage: The Guided 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 WP 5x10 mm Single-Pat - Product Usage: Drills 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: Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: 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: Drill Tapered RP 4.3x11.5 mm Single-Pat - Product Usage: The 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 NP 3.5x11.5 mm Single-Pat - Product Usage: The 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: Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided...
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: 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: 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: 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: 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: 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 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: 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.