Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 968 recalls have been distributed to Michigan in the last 12 months.
Showing 40161–40180 of 53,342 recalls
Recalled Item: Fentanyl 5 Recalled by The Compounding Pharmacy of America Due to Lack of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone 40 mg/ml + Bupivacaine 40 mg/ml Solution Recalled by The...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone 35 mg/ml + Bupivacaine 10 mg/ml + Baclofen 1 Recalled by The...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin 1 Recalled by The Compounding Pharmacy of America Due to...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 40 mg/ml (10 ml Sesame Oil) Recalled by The...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bi-Mix Medium (30/1) Injectable Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix (22.5/0.83/8.3) Injectable Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bi-Mix (20/1) Injectable Recalled by The Compounding Pharmacy of America Due...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyaluronic Acid Sodium 32 mg/ml + Lidocaine HCl 3 mg/ml Injection Recalled...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: 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: 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: 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.