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. 913 recalls have been distributed to Idaho in the last 12 months.
Showing 43781–43800 of 48,215 recalls
Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...
The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...
The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...
The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...
The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...
The Issue: Hospira has received reports of customers experiencing air-in-line alarms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHAMPION Medical Recliner Recalled by Invacare Corporation Due to There is a...
The Issue: There is a possibility of elevated temperatures in the seat pad. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Theraflu Exte (dextromethorphan hydrobromide 20 mg Recalled by Novartis...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-Release Capsules (LA) Recalled by...
The Issue: Failed Dissolution Specifications: Product is being recalled due to out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-Release Capsules (LA) Recalled by...
The Issue: Failed Dissolution Specifications: Product is being recalled due to out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Nighttime Severe Cold & Cough (acetaminophen 650 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Discoloration: This recall is being carried out due to an orange to brown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Flu & Chest Congestion (acetaminophen 1000 mg and guaifenesin...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NeoCitran Extra Strength Non-Drowsy Cold & Sinus (acetaminophen 650 mg...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Flu & Sore Throat (acetaminophen 650 mg Recalled by Novartis...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.