Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,073 recalls have been distributed to Iowa in the last 12 months.
Showing 14121–14140 of 49,990 recalls
Recalled Item: CSF Otic Insufflation Capsule Recalled by Edge Pharma, LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tetracaine HCl Nasal Solution Recalled by Edge Pharma, LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Recalled by Edge Pharma, 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: Profound-PE Dental Gel Recalled by Edge Pharma, LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx21 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx7 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: investigation into a customer complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw Recalled by Wright...
The Issue: Incorrect product is contained in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker DARCO Screw Recalled by Wright Medical Technology Inc Due to The...
The Issue: The incorrect product is contained in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...
The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker CLAW II ORTHOLOC 3DSi Plate Recalled by Wright Medical Technology...
The Issue: The incorrect product is contained in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUBS Naturals Fountain of Youth Formula Recalled by Slayer Forever, LLC dba...
The Issue: Supplement contains undeclared milk from MCT oil powder ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.