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 10041–10060 of 49,990 recalls
Recalled Item: PrimeZEN Black 6000 capsule Recalled by Volt Candy Wholesale Club Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Global Total LP single step medium Recalled by CooperSurgical, Inc. Due to...
The Issue: It has come to CooperSurgical's attention that the affected Product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to Firm has...
The Issue: Firm has initiated a removal of the product due to insufficient evidence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by B. Braun Medical Inc. Due to Lack...
The Issue: Lack of sterility assurance: Recall of certain batches of 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by B. Braun Medical Inc. Due to Lack...
The Issue: Lack of sterility assurance: Recall of certain batches of 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips DreamStation Auto BiPAP and CPAP Recalled by Philips Respironics,...
The Issue: A limited number of remediated Philips DreamStation units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed 7.0 Recalled by...
The Issue: Due to potential leaks associate with the Oral/Nasal Tracheal Tube Cuffed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensus Healthcare Inc Recalled by Sensus Healthcare, Inc. Due to When the...
The Issue: When the user pauses the beam delivery, the dose timer is reset (to zero),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II ROODRA non-invasive vascular diagnostic device Recalled...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II REVO non-invasive vascular diagnostic device Recalled by...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: allergy relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: allergyrelief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: allergy relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.