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. 2,494 recalls have been distributed to Minnesota in the last 12 months.
Showing 22601–22620 of 29,186 recalls
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...
The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...
The Issue: Wands inspected with the adaptor fixture were released to the field not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...
The Issue: Insufficient seal on the outside packaging, potentially affecting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Access System Recalled by Stryker Sustainability Solutions Due to...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laksell GammaPlan Recalled by Elekta, Inc. Due to Memory can become...
The Issue: Memory can become corrupted when creating a fused study via drag and drop in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fios First Entry Recalled by Stryker Sustainability Solutions Due to Stryker...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 620. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 630. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA DX-D 100 is a mobile digital radiography x-ray system Recalled by AGFA...
The Issue: When using the DX-D 100 unit, sporadic unintended movements caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.