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. 2,590 recalls have been distributed to Iowa in the last 12 months.
Showing 12001–12020 of 28,127 recalls
Recalled Item: OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION 3CC IMPACTFORMULA. REF/UDI: 390-2103/00813845020078 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 3CC IMPACTFORMULA. REF/UDI: 390-0203/00813845020030 - Product...
The Issue: Incorrect shelf-life for bone void filler kits; the product may not maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator APS Aliquoter Module Recalled by Abbott Laboratories Due to In...
The Issue: In the case of an AQM clot detection error a portion of the distilled water...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001...
The Issue: During Giraffe Shuttle charging, the batteries emit low concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRESTIGE RETRACTION GRASPER Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Endoscopic graspers may become separated at the weld from handle to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION Recalled by Aesculap Implant...
The Issue: Endoscopic graspers may become separated at the weld from handle to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CKMB Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The Spanish and Swedish language versions of the IFU state that the assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CKMB Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The Spanish and Swedish language versions of the IFU state that the assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bridge Occlusion Balloon Recalled by Spectranetics Corporation Due to There...
The Issue: There is a potential for thrombus formation on balloons prepped and staged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US) Recalled by...
The Issue: False positive reaction on the reagent.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem¿VELOCITY Urine Chemistry System- Recalled by Beckman Coulter Inc. Due...
The Issue: A defect in the SATA power adapter cable within the instruments computer has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ200 Series Urine Microscopy Analyzer- All part numbers Recalled by Beckman...
The Issue: A defect in the SATA power adapter cable within the instrument s computer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MoXy Laser Fiber Recalled by Boston Scientific Corporation Due to To...
The Issue: To reinforce existing instructions within the Directions for Use (DFU) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leksell Vantage Stereotactic System. Instrument Carrier Recalled by Elekta...
The Issue: A faulty locking piece of the Instrument Carrier that does not fulfil the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Oxymetry Oligon Catheter Kit. Pressure injectable....
The Issue: Sterile catheter kit packaging compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...
The Issue: In affected software version, of Positron emission tomography and computed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628...
The Issue: Nonconforming product; length of the product measured shorter than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.