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. 2,507 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,507 in last 12 months

Showing 3676136780 of 53,342 recalls

Medical DeviceFebruary 29, 2016· Richard Wolf Medical Instruments Corp.

Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...

The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...

The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm has received one report of values for patient height and weight...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...

The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...

The Issue: Dialyzer header leak due to possible improper torque

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 26, 2016· Rich Products Corp

Recalled Item: New York Style Chocolate Iced ¿clairs under the following labels: Recalled...

The Issue: Products were recalled due to the potential presence of plastic foreign...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2016· Torrent Pharmaceuticals Limited

Recalled Item: Telmisartan Tablets Recalled by Torrent Pharmaceuticals Limited Due to...

The Issue: Presence of Foreign Substance: Product complaint for the presence of foreign...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· Scottcare Corporation

Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...

The Issue: The firm received a complaint of the battery exploding while recharging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Product Usage: Rebound Cartilage is an external knee...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing