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. 2,532 recalls have been distributed to Michigan in the last 12 months.
Showing 27581–27600 of 53,342 recalls
Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spring-Wire Guide Introducer Catheter Assembly Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NvisionVLE¿ Low-Profile Optical Probe Recalled by Ninepoint Medical Inc. Due...
The Issue: Distal tips of the probes may detach from the probe shaft during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit for the Preparation of Technetium TC-99M Mebrofenin Recalled by...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liberty Snacks Raw ALMONDS Net Wt. 1.3 oz (#g) DISTRIBUTED Recalled by Ohio...
The Issue: The firm received positive test results for Listeria monocytogenes in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By Heinens Recalled...
The Issue: The firm received positive test results for Listeria monocytogenes in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liberty Snacks NUTS ALMOND RAISIN Mix Net Wt. 1.6 oz Recalled by Ohio...
The Issue: The firm received positive test results for Listeria monocytogenes in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liberty Snacks Honey Roasted CASHEWS Net Wt. 1.2 oz (#g) Recalled by Ohio...
The Issue: The firm received positive test results for Listeria monocytogenes in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liberty Snacks Natural PISTACHIOS Net Wt. 1 oz (#g) DISTRIBUTED Recalled by...
The Issue: The firm received positive test results for Listeria monocytogenes in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hickory Harvest Island Fruit Mix NET WT 9 oz (255g) Recalled by Ohio Hickory...
The Issue: The firm received positive test results for Listeria monocytogenes in a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for adhesive transfer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Angio-Seal Evolution Vascular Closure Device Recalled by Terumo Medical Corp...
The Issue: Two lots of product were released for distribution prior to the completion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...
The Issue: There is a supplier quality issue with the terminal blocks which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit Recalled by VGI...
The Issue: IFU contained an automated cleaning process for the VerteLP Instrument Tray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING Recalled by Smith &...
The Issue: A single lot of GENESIS II FEMORAL FIVE DEGREE VALGUS BUSHING due to a laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.