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. 2,645 recalls have been distributed to Michigan in the last 12 months.
Showing 17341–17360 of 53,342 recalls
Recalled Item: Brain Heart Infusion Agar with 6 ug/ml Vancomycin Cat no: Recalled by Hardy...
The Issue: Complaints were received reporting of Staphylococcus aureus (ATCC 29213)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....
The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...
The Issue: Shipping box may contain wrong model.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzhydrocodone and Acetaminophen Tablets Recalled by KVK-Tech, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...
The Issue: Misleading error messages and a gap in the Operator Manual which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...
The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...
The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit (LCSU 4) Recalled by Laerdal Medical (Suzhou)...
The Issue: Component failures may cause the unit to lose all suction. Users will need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnshLabs - SARS-CoV2 IgM ELISA (u-Capture) Recalled by Ansh Labs, LLC Due to...
The Issue: Labeling update; To reduce the risk of false positive/false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: morphine sulfate 150 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Recalled by SCA Pharmaceuticals Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product confirmed to have yeast
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esmolol HCl 100 mg/10 mL (10mg/ mL) Recalled by SCA Pharmaceuticals Due to...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 10mg/50mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate 50 mg/10mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 5000 mg/50 mL in Sodium Chloride 0.9% (100 mcg/mL) Rx Only...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine 25 mg/5 mL in 0.9% Sodium Chloride Injection Recalled by SCA...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 100 mcg/50mL Ropivacaine HCl 0.1% in 0.9% Sodium Chloride 50 mL...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Citrate 4% 3 mL Anticoagulation Solution (40mg/mL) Recalled by SCA...
The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.