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. 2,618 recalls have been distributed to Iowa in the last 12 months.
Showing 10221–10240 of 49,990 recalls
Recalled Item: SIEMENS Biograph Vision: a) 450 Recalled by Siemens Medical Solutions USA,...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g Recalled by Eastland Food...
The Issue: Cashews declared in ingredients statement but not in the contains statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by SUN...
The Issue: Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S2 Racepinephrine Inhalation Solution Recalled by Nephron Sc Inc Due to...
The Issue: Short Fill
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator (racephedrine...
The Issue: Short Fill
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allopurinol Tablets USP Recalled by Accord Healthcare, Inc. Due to Presence...
The Issue: Presence of Foreign Substance: Presence of a small piece of green plastic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Nephron Sc Inc Due to CGMP...
The Issue: CGMP Deviations: potential for trace amounts of product carryover.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Nephron Sc Inc Due to CGMP...
The Issue: CGMP Deviations: potential for trace amounts of product carryover.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fiber Powder Recalled by Ortho Molecular Products, Inc. Due to Raw material...
The Issue: Raw material tested positive for Cronobacter sakazakii.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Amerisource Health...
The Issue: Failed Dissolution Specifications: This recall is being initiated in support...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Humatrix Microclysmic Gel Recalled by Consolidated Chemical, Inc Due to CGMP...
The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Techni-Care Chloroxylenold 3% Recalled by Consolidated Chemical, Inc Due to...
The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.