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. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 25081–25100 of 28,127 recalls
Recalled Item: STERRAD 100NX Cassettes The STERRAD Sterilization System is a low Recalled...
The Issue: Advanced Sterilization Products (ASP) is recalling the three lots (13F049,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Homocysteine Flex Reagent Cartridge The HCYS method...
The Issue: Dimension Vista HCYS lot 13064MA shows erratic recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Brivo OEC715/785/865 C-Arm Recalled by GE Healthcare Beijing , Hangwei...
The Issue: GE is recalling certain lots of GE Brivo OEC715/785/865 C-Arm due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Individual units labeled in part: Recalled by Richard Wolf Medical...
The Issue: Richard Wolf Medical Instrument Corporation recieved a complaint stating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 200 Sterilizer (Single Door) Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius (TM) TEMPERATURE THERAPY Recalled by DeRoyal Industries Inc Due to...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...
The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...
The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower...
The Issue: PENTAX Medical has become aware of a product issue associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.