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. 2,520 recalls have been distributed to Michigan in the last 12 months.
Showing 29821–29840 of 53,342 recalls
Recalled Item: CS 100i Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...
The Issue: False blood back detection alarm and the ingress of fluids into the IABP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: New Kopi Jantan Tradisional Natural Herbs Coffee Recalled by BESTHERBS...
The Issue: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NatureBox Sticks 'n Stones Recalled by NatureBox, Inc. Due to Firm received...
The Issue: Firm received notification that a consumer found a peanut in NatureBox...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RayStation Product Usage: is a software system designed for treatment...
The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TD60 Transmitter battery charger used with the BeneVision Central Station...
The Issue: A damaged circuit board in the battery charger can cause the battery to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...
The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHENYLephrine 50 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2 mcg/mL + BUPIvacaine 0.1% PF in 0.9% NS 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Fill in 3 mL BD syringe...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAGNESIUM Sulfate 4 g added to 100 mL 0.9% Sodium Chloride Recalled by SCA...
The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine 20 mg in 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ephedrine Sulfate in 0.9% Sodium Chloride 10 mL Recalled by Cantrell Drug...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium Chloride 250 Recalled by...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag Recalled by...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine sulfate 1 mg per mL in 0.9% Sodium Chloride Recalled by SCA...
The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.