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 28561–28580 of 49,990 recalls
Recalled Item: BUPIVacaine HCl 0.1% PF (From 0.75%) in 0.9% Sodium Chloride Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride 20 meq Added to Sodium Chloride 0.9% 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 25 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine 100 mg in 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 3 mcg/mL + BUPIvacaine 0.1% in 0.9% Sodium Chloride 250 mL Recalled...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride Recalled by SCA...
The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...
The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TD60 Transmitter battery charger used with the BeneVision Central Station...
The Issue: A damaged circuit board in the battery charger can cause the battery to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.