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. 2,428 recalls have been distributed to Iowa in the last 12 months.
Showing 33061–33080 of 49,990 recalls
Recalled Item: cobas 6800/8800 system Hepatitis Viral B DNA Detection Product Usage:...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Articulating Linear Cutter Recalled by Ethicon Endo-Surgery Inc...
The Issue: Quality control identified a component issue where the pinion gear in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Articulating Linear Cutter Recalled by Ethicon Endo-Surgery Inc...
The Issue: Quality control identified a component issue where the pinion gear in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative Recalled...
The Issue: Microbial contamination of Non-Sterile Products; positive findings of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol Recalled...
The Issue: Failed Content Uniformity Specifications: out of specification test result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...
The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molly's Kitchen Hotzzarella Cheese Sticks Recalled by Ajinomoto Windsor...
The Issue: Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poppers brand Mozzarella Cheese Sticks Net Wt. 32 oz. (2 Recalled by...
The Issue: Monogram Appetizers is recalling Poppers Brand Mozzarella Cheese Sticks...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...
The Issue: The STAT priority icon was not displayed in the Study List when the study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in...
The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.