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. 2,464 recalls have been distributed to Iowa in the last 12 months.
Showing 22781–22800 of 28,127 recalls
Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...
The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...
The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPath Laboratory Information System. Versions 4.3.0.8 Recalled by SCC...
The Issue: Modifications to diagnostic text may be: 1) Saved to the database but not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...
The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE 46-SERIES Medical Washer-Disinfector Recalled by Getinge...
The Issue: Getinge Disinfection AB received complaints regarding sediment residuals in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer PERSONA Tibial Articular Surface Inserter Recalled by Zimmer, Inc....
The Issue: Potential for fracture of the tip of the product. The fractured tip is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: While servicing a unit at a customer site, a field engineer discovered a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...
The Issue: A configuration update needs to be done on TactiSys to appropriately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoject E1 Fixed needle device Recalled by Owen Mumford USA, Inc. Due to...
The Issue: The syringe carrier is missing components: a damper and spring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device 20G x1 Recalled by Smiths Medical...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...
The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone Screw Recalled by Zimmer Manufacturing B.V. Due to Analysis of returned...
The Issue: Analysis of returned complaint devices, product in inventory, and device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL PT-Fibrinogen HS PLUS Recalled by Instrumentation Laboratory Co. Due...
The Issue: Some vials of HemosIL PT-Fibrinogen HS PLUS, Part No. 0008469810 (various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.