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 25681–25700 of 49,990 recalls
Recalled Item: Revolution CT systems with the SmartStep Option The system is Recalled by GE...
The Issue: On the Revolution CT systems equipped with the SmartStep Option, the Z...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Recalled by...
The Issue: Dental varnish has the possibility of having an unpleasant and off flavor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...
The Issue: Presence of Particulate Matter: organic and inorganic compounds detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent Drug and Failed Stability Specifications: lot out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Failed...
The Issue: Failed Stability Specifications: lot out of specification for elevated water...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent Drug: lots out of specification for elevated sodium chloride and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...
The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P400 PREM U/M 18FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEMP SENSE SILICONE 14FR5CC2W Recalled by COVIDIEN LLC Due to The...
The Issue: The temperature sensor catheters may be defective in that they will show a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.