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 31841–31860 of 53,342 recalls
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...
The Issue: An unexpected transient mode switch behavior was detected by Medtronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...
The Issue: An extremely dusty computer can cause problems at system start, or rarely,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...
The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...
The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI . The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Bakery Peanut Butter Chocolate Chunk Cookies Recalled by Jimmy's Cookies...
The Issue: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EasyCAL HbA1c Calibrator Recalled by Medica Corporation Due to Patient...
The Issue: Patient results determined using this calibrator lot might deviate up to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...
The Issue: Some anomalies have been identified during manufacturing controls.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys PreciControl Varia 3 Recalled by Roche Diagnostics Corporation Due...
The Issue: e-barcode and value sheet for PreciControl Varia contains a typographical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....
The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional...
The Issue: Potential Patient Demographic Error with Blank Patient ID Field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...
The Issue: The current secondary packaging, a box, incorrectly states that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate (Preservative Free) 10 mcg per mL (1 Recalled by PharMedium...
The Issue: Labeling: Not Elsewhere Classified- Diluent used to compound product expired...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate (Preservative Free) 20 mcg per mL (2 Recalled by PharMedium...
The Issue: Labeling: Not Elsewhere Classified- Diluent used to compound product expired...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estrone Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...
The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...
The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.