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. 2,634 recalls have been distributed to Iowa in the last 12 months.
Showing 5621–5640 of 49,990 recalls
Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...
The Issue: The adjustment ring on the device may become loose resulting in the wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...
The Issue: Some of the devices may function incorrectly resulting in no temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Simultaneous ECG measurements with multiple devices, including a manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Defective container: lack of seal integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...
The Issue: There is a potential for the top cover of the hospital bed mattress to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...
The Issue: System monitor screen may display atypical behavior: Overlapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...
The Issue: Reports of patient burns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...
The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release...
The Issue: Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by MACLEODS...
The Issue: Presence of foreign substance: plastic-like substance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Impact Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv. Hemostasis...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360/A+ spare batteries. Item Number: SUB0000864. Recalled by ICU...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000864 Recalled by ICU Medical Inc Due...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.