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. 2,551 recalls have been distributed to Idaho in the last 12 months.
Showing 12361–12380 of 48,215 recalls
Recalled Item: Open Nature Cough Drops Menthol-Cough Suppressant/Oral Anesthetic Peppermint...
The Issue: Subpotent drug: Low OOS for menthol content at the three month room temperature.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GaviLyte -C (Polyethylene Glycol 3350 Recalled by Lupin Pharmaceuticals Inc....
The Issue: Failed Stability Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEG 5000 Functional Fibrinogen Reagent Recalled by Haemonetics Corporation...
The Issue: Due to a shift in the citrated blood range for a normal population, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Wet -Field Eraser Recalled by Beaver Visitec International, Inc. Due to...
The Issue: Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin HCl 1.5 g in 0.9% Sodium Chloride Recalled by SCA Pharmaceuticals...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag Recalled by SCA...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules USP Recalled by Glenmark Pharmaceuticals Inc., USA Due...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...
The Issue: Device did not pass electrical safety testing for adequate insulation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 10 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 20 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accupril (Quinapril HCl Tablets) 40 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.