Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,544 recalls have been distributed to Idaho in the last 12 months.
Showing 11561–11580 of 27,833 recalls
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health NPWT Canister with Gel 300cc Recalled by Cardinal Health...
The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health NPWT Occlusion Detection Canister 300cc Recalled by Cardinal...
The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrimeStore Molecular Transport Medium (PS-MTM) Recalled by LONGHORN VACCINES...
The Issue: The tubes may have been delivered to some users without labels. Users may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 96 Instrument Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: When using Sample Transfer protocol version 3.0, the drop catcher is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COOPERSURGICAL Os FinderTM Cervical Dilator Recalled by CooperSurgical, Inc....
The Issue: Mislabeled: Printing on the top web or Tyvek lid of the individual product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America, LLC Due to Thermo...
The Issue: Thermo switches in the main power supply for the system may be incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by TELEFLEX MEDICAL INC Due to Teleflex is...
The Issue: Teleflex is initiating a voluntary recall for the above-mentioned products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.