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 26841–26860 of 49,990 recalls
Recalled Item: PRIMUS HI Recalled by Siemens Medical Solutions USA, Inc Due to Control...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M2 / PRIMUS Mid-Energy Recalled by Siemens Medical Solutions USA,...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Avant-garde Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Expression Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valacyclovir Tablets USP 1 gram Recalled by Hetero Labs Limited Unit V Due...
The Issue: Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valganciclovir Tablets Recalled by Hetero Labs Limited Unit V Due to...
The Issue: Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Acetate Capsules Recalled by Nostrum Laboratories Inc Due to...
The Issue: Presence of Foreign Tablets/Capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaPET¿ RF Latex Reagent used as a component in the Recalled by Stanbio...
The Issue: All patient serum samples yield a weakly positive test result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK¿ PROG III Recalled by Tosoh Bioscience Inc Due to Falsely...
The Issue: Falsely elevated progesterone assay values will occur when using certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK¿ PROG II Recalled by Tosoh Bioscience Inc Due to Falsely...
The Issue: Falsely elevated progesterone assay values will occur when using certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled:...
The Issue: The duodenoscopes are being recalled in order to replace the forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grape Fanta Recalled by Heartland Coca-Cola Bottling Company Due to Sharp...
The Issue: Sharp edges were observed on several of the cans which have the potential of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pibb Zero Recalled by Heartland Coca-Cola Bottling Company Due to Sharp...
The Issue: Sharp edges were observed on several of the cans which have the potential of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diet Coke Lime Recalled by Heartland Coca-Cola Bottling Company Due to Sharp...
The Issue: Sharp edges were observed on several of the cans which have the potential of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sprite Zero Recalled by Heartland Coca-Cola Bottling Company Due to Sharp...
The Issue: Sharp edges were observed on several of the cans which have the potential of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caffeine Free Coke Zero Recalled by Heartland Coca-Cola Bottling Company Due...
The Issue: Sharp edges were observed on several of the cans which have the potential of...
Recommended Action: Do not consume. Return to store for a refund or discard.