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. 911 recalls have been distributed to Idaho in the last 12 months.
Showing 44981–45000 of 48,215 recalls
Recalled Item: Dermalight 80 Model Number UVB-080 Recalled by National Biological Corp Due...
The Issue: The incorrect manual may have been packaged with this product. UVB-080...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (No Brand) First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M Tekk Brand Industrial/Construction First Aid Kit Recalled by Total...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medi-First Brand First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Aurobindo Pharma USA Inc Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: Incorrect strength on side...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defribillator Recalled by Philips Healthcare Inc. Due...
The Issue: Device may fail to deliver defibrillation therapy in either Manual Defib or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endopath Electrosurgery Probe Plus II Recalled by Ethicon Endo-Surgery Inc...
The Issue: The firm is recalling the ENDOPATH Probe Plus II Shafts because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid Recalled by...
The Issue: Review of validation information and customer complaints which indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Gabapentin Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Gabapentin Sodium tablets is recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Topiramate Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Topiramate Tablets is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Pravastatin Sodium Tablets Recalled by Glenmark Generics Inc., USA...
The Issue: Chemical Contamination: Pravastatin Sodium Tablets isbeing recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling
The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software correction applies to customers who use the RT Therapist Recalled...
The Issue: Software update to fix multiple safety related issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS PANELS Recalled by Polymer Technology Systems, Inc. Due to Internal...
The Issue: Internal investigation demonstrated under-recovery for glucose when tested...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.