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. 966 recalls have been distributed to Idaho in the last 12 months.
Showing 33601–33620 of 48,215 recalls
Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...
The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...
The Issue: Eye Station images were not importing properly and were imported under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...
The Issue: The software did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...
The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...
The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...
The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine 75 mg Tablet Recalled by Bryant Ranch Prepack Inc. Due to...
The Issue: Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection USP Recalled by B. Braun Medical Inc Due to...
The Issue: Non-Sterility: fungal contamination due to leaking containers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...
The Issue: Incorrect expiration date was printed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...
The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...
The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...
The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GERBER Organic 2ND FOODS¿ Carrots Recalled by Nestle Infant Nutrition Due to...
The Issue: Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GERBER Organic 2ND FOODS Pears Recalled by Nestle Infant Nutrition Due to...
The Issue: Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿...
Recommended Action: Do not consume. Return to store for a refund or discard.