Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,650 recalls have been distributed to Minnesota in the last 12 months.
Showing 8401–8420 of 52,120 recalls
Recalled Item: Lettuce Romaine 80/20 GB Recalled by G.O. Corporation Due to Romaine lettuce...
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lett. Blend Rom/End/Rad-All Seasons packaged in the following sizes and...
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lettuce Romaine All American Recalled by G.O. Corporation Due to Romaine...
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Romaine lettuce packaged into the following configurations and sizes: 1....
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lett. Salad Shred Mix w/Rom Recalled by G.O. Corporation Due to Romaine...
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lettuce Rom Blend 50/50 Recalled by G.O. Corporation Due to Romaine lettuce...
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: COOLIEF RF Generator is an 80-watt Radio-Frequency (RF) Generator with...
The Issue: Avanos has received an increase in complaints from customers for COOLIEF RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The incorrect product labeling was applied to the product indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were identifying autofill failure conditions on the devices causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were identifying autofill failure conditions on the devices causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.