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 27021–27040 of 29,286 recalls
Recalled Item: Part 510636 Disposable Infusion Pump Recalled by Symbios Medical Products,...
The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 510076 Disposable Dual Infusion Pump Recalled by Symbios Medical...
The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 510121 Disposable Infusion Pump Recalled by Symbios Medical Products,...
The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 510031 Disposable Single Infusion Pump Recalled by Symbios Medical...
The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part510447 Disposable Infusion Pump Recalled by Symbios Medical Products,...
The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invue Split Driver Recalled by SpineFrontier, Inc. Due to Device design.
The Issue: Device design.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multilite Dye Handpieces Recalled by ConBio, a CynoSure Company Due to An...
The Issue: An inconsistency was identified related to electronic display identification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra PANTA Arthrodesis Nail System. Intended for use in...
The Issue: As a result of the investigation into an adverse trend of complaints for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRP Slides (Reagent) Recalled by Ortho-Clinical...
The Issue: While performing interval testing Ortho Clinical Diagnostics (OCD)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products K+ (Potassium) Slides (Reagent) Recalled by...
The Issue: While performing interval testing, Ortho Clinical Diagnostics (OCD)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS versions 7.4 Recalled by Novarad Corporation Due to Potential for...
The Issue: Potential for images to be flipped while streaming, which could incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy LifeLiner Stick & Cut Resistant Gloves Rt Recalled by DePuy...
The Issue: LifeLiner Stick and Cut Resistant Gloves are being recalled because cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...
The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...
The Issue: Intuitive Surgical has identified a potential for some units of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...
The Issue: Potential for set screw to be come deformed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.