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. 2,622 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,622 in last 12 months

Showing 2050120520 of 53,342 recalls

FoodDecember 19, 2019· Almark Foods, LLC

Recalled Item: White Medium Hard Cooked Eggs w/Salt & Pepper sold under Recalled by Almark...

The Issue: The firm was notified by FDA & CDC of a potential Listeria monocytogenes...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Almark Foods, LLC

Recalled Item: PECKISH PERFECTLY BOILED FREE RANGE ORGANIC Egg Salt & Pepitas Recalled by...

The Issue: The firm was notified by FDA & CDC of a potential Listeria monocytogenes...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Almark Foods, LLC

Recalled Item: Vital Farms Pasture Raised Hard Cooked Eggs w/Salt & Pepper Recalled by...

The Issue: The firm was notified by FDA & CDC of a potential Listeria monocytogenes...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Almark Foods, LLC

Recalled Item: PECKISH PERFECTLY BOILED FREE RANGE ORGANIC Egg Everything Bagel Flavor...

The Issue: The firm was notified by FDA & CDC of a potential Listeria monocytogenes...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Almark Foods, LLC

Recalled Item: Frozen Diced Eggs sold under the brand names of Almark Foods Recalled by...

The Issue: The firm was notified by FDA & CDC of a potential Listeria monocytogenes...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Almark Foods, LLC

Recalled Item: Almark Foods Smokehouse ProBox Mini White Medium Hard Cooked Eggs Recalled...

The Issue: The firm was notified by FDA & CDC of a potential Listeria monocytogenes...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Whole Foods Market

Recalled Item: 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes Recalled...

The Issue: Potential to contain undeclared milk and coconut.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Whole Foods Market

Recalled Item: 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes Net Wt Recalled...

The Issue: Potential to contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Smith & Nephew, Inc.

Recalled Item: LEGION PS High Flex XLPE size 5-6 9mm Articular Insert Recalled by Smith &...

The Issue: LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Randox Laboratories, Limited

Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...

The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...

The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Zimmer Biomet, Inc.

Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...

The Issue: Potential issue associated with the instrument -end of the shaft could fail...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Enzymatic Creatinine (ECREA) reagent Recalled by Siemens...

The Issue: There is a potential for falsely depressed creatinine results for patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing