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. 1,820 recalls have been distributed to Iowa in the last 12 months.
Showing 32701–32720 of 49,990 recalls
Recalled Item: Ephedrine Sulfate Injection Recalled by Sandoz Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCI Injection Recalled by Sandoz Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...
The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...
The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...
The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...
The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...
The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...
The Issue: Casters on the EKOS carts may be missing washers which can cause premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...
The Issue: Incorrect label on the Sertera Biopsy Kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to...
The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...
The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.