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.

53,342 total recalls
2,520 in last 12 months

Showing 2646126480 of 29,286 recalls

Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX" Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID" Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Recalled by Smith & Nephew, Inc. Endoscopy...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra PLLA/HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Straight Recalled by Smith & Nephew, Inc....

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company - Health Care Business

Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...

The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...

The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing