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. 2,488 recalls have been distributed to Iowa in the last 12 months.
Showing 21441–21460 of 49,990 recalls
Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...
The Issue: The threads on posts stripping out when tensioned during application process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Revelation with software version VC10 and Biopsy Option Intended...
The Issue: An error can occur when performing a biopsy using the InSpect function. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...
The Issue: Inaccurately Low Sample Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...
The Issue: Inaccurately Low Sample Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...
The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...
The Issue: Reversed expiration and manufacturing date on the label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...
The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...
The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...
The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresket Thai Lobster Salad packaged in 5lb plastic container Recalled by...
The Issue: Listeria monocytogenes was found in egg salad produced by the firm. In...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresket egg salad packaged in 32oz plastic cup with lid Recalled by...
The Issue: Listeria monocytogenes was found in egg salad produced by the firm. In...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresket Tuna Salad packaged in 5lb plastic container Recalled by Elevation...
The Issue: Listeria monocytogenes was found in egg salad produced by the firm. In...
Recommended Action: Do not consume. Return to store for a refund or discard.