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 5981–6000 of 28,127 recalls
Recalled Item: UFSK Treatment chair 500 XLE- Treatment chair for positioning and Recalled...
The Issue: Service life of the electrical seat part drive of the treatment chair may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Specific...
The Issue: Specific diluent lot numbers showed that conductivity, osmolality, and pH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (Agar) (150mm) Recalled by Remel, Inc Due to...
The Issue: The test medium may not perform as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Resurfacing Cup - (xx)MM Recalled by Synovo Production Due to...
The Issue: Medical device components were marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACETABULAR FIXATION CUP Recalled by Synovo Production Due to Medical device...
The Issue: Medical device components were marketed without FDA clearance and without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020 Recalled by Synovo...
The Issue: Medical device components were marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module Recalled by Abbott Laboratories Due...
The Issue: There are potential performance issues found in the Alinity ci-series System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs...
The Issue: Weld protrusion/physical gap between the housing and pack cover, may exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) OPEN HEART TRACECART Recalled...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) PELVIC EXAM TRAY Recalled by...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.800 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.500 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Recalled by...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.