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. 2,614 recalls have been distributed to Idaho in the last 12 months.
Showing 2921–2940 of 48,215 recalls
Recalled Item: Baxter Floor mounting column TS 7500 U Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...
The Issue: There is a software issue which causes the upper back section to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...
The Issue: Chemical Contamination: Presence of benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Peanut Butter Protein Balls. Product has expected life of Recalled...
The Issue: Undeclared soy lecithin and undeclared color additives Blue 1 Lake, Yellow...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...
The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...
The Issue: In situations where two images with differing Fields of View (FOV) complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing...
The Issue: Lack of Assurance of Sterility: due to a quality control process deviation....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.