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. 2,549 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,549 in last 12 months

Showing 2586125880 of 53,342 recalls

Medical DeviceJuly 26, 2018· Stryker GmbH

Recalled Item: Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: Recalled...

The Issue: When creating a correction plan with the Correct Axial First button selected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2018· Steris Corporation

Recalled Item: AMSCO V-PRO 1 Recalled by Steris Corporation Due to There is the potential...

The Issue: There is the potential for a scenario where a punctured cup of sterilant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2018· Covidien LLC

Recalled Item: Li-ion battery packs used in BIS Vista and BIS View Recalled by Covidien LLC...

The Issue: Revised replacement instructions for the Li-ion battery packs used in BIS...

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

Class II — Potential Health HazardOngoing
DrugJuly 25, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray...

The Issue: Presence of foreign substance: Potential for glass in the neck area of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 25, 2018· Med-Mizer, Inc.

Recalled Item: PR1000 Pivot Rehab Bed AC powered adjustable bed. Recalled by Med-Mizer,...

The Issue: Under certain conditions, when pivoting bed to the extreme left there are...

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

Class II — Potential Health HazardOngoing
DrugJuly 24, 2018· West-Ward Columbus Inc

Recalled Item: Doxycycline Hyclate Tablets Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Dissolution Specifications:

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2018· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Morton Grove...

The Issue: Defective Container: Tamper Evident foil seal not completely intact.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2018· West-Ward Columbus Inc

Recalled Item: Doxycycline Hyclate Tablets Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Dissolution Specifications:

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2018· KRAFT HEINZ FOODS COMPANY

Recalled Item: Taco Bell Salsa Con Queso Mild 15oz retail jar Recalled by KRAFT HEINZ FOODS...

The Issue: Product is at risk for growth of Clostridium botulinum

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2018· K2M, Inc

Recalled Item: YUKON Polyaxial Screws (3.5 X 12 mm Recalled by K2M, Inc Due to Screws had a...

The Issue: Screws had a manufacturing error that could prevent the screw from mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM CKMB Calibrator Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: A potential bias was identified with certain kits compared to the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CKMB Calibrator Recalled by Siemens Healthcare Diagnostics,...

The Issue: A potential bias was identified with certain kits compared to the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM CKMB Master Curve Material Recalled by Siemens Healthcare...

The Issue: A potential bias was identified with certain kits compared to the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CKMB Master Curve Material Recalled by Siemens Healthcare...

The Issue: A potential bias was identified with certain kits compared to the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CKMB Calibrator 2-pack Japan Recalled by Siemens Healthcare...

The Issue: A potential bias was identified with certain kits compared to the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE...

The Issue: BioFlo Ports was partially manufactured with the incorrect sterile port...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Diagnostica Stago, Inc.

Recalled Item: Diagnostica Stago STA N¿oplastine¿ CI Recalled by Diagnostica Stago, Inc....

The Issue: QC values outside of the assigned ranges (prolonged Prothrombin time /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Diagnostica Stago, Inc.

Recalled Item: Diagnostica Stago STA N¿oplastine¿ CI Plus Recalled by Diagnostica Stago,...

The Issue: QC values outside of the assigned ranges (prolonged Prothrombin time /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Mako Surgical Corporation

Recalled Item: Stryker Mako Vizadisc Knee Procedure Tracking Kit Recalled by Mako Surgical...

The Issue: Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Mako Surgical Corporation

Recalled Item: Stryker Mako Vizadisc Hip Procedure Tracking Kit Recalled by Mako Surgical...

The Issue: Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip...

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

Class II — Potential Health HazardOngoing