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 35401–35420 of 48,215 recalls
Recalled Item: Piracetam Injection Recalled by Downing Labs, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DMPS Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chromium Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin Buffered Injectable Recalled by Downing Labs, LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate 50% Injectable Recalled by Downing Labs, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Tryptophan Injectable Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Taurine Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thiotic Acid Injection Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Glutathione Injection Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG (Lyophilized) Injectable Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDTA Calcium Disodium Injectable Recalled by Downing Labs, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetyl-L-Carnitine Injectable Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Arginine Injection Recalled by Downing Labs, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...
The Issue: Complaint investigation concluded that although product quality requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...
The Issue: It was reported that packaging was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.