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. 2,571 recalls have been distributed to Iowa in the last 12 months.
Showing 14241–14260 of 28,127 recalls
Recalled Item: Canon Aquilion One Vision Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion Premium Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...
The Issue: New software version for affected ventilators reduces the probability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...
The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Standard Base Recalled by Community Products, LLC Due to A...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Low Base Recalled by Community Products, LLC Due to A design...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable Pump Recalled by Flowonix Medical Inc Due to The pump...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Clinician Programmer (Touchscreen) Software version 2.00.29...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmer (Grand Prime) Software version 2.00.29 Recalled by...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump Recalled by Flowonix Medical Inc Due to The...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.