Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,503 in last 12 months

Showing 1558115600 of 27,462 recalls

Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Manual) Recalled by FHC, Inc. Due to The...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Anika Therapeutics, Inc.

Recalled Item: Hyalomatrix Recalled by Anika Therapeutics, Inc. Due to Hyalomatrix products...

The Issue: Hyalomatrix products are susceptible to degradation as a result of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: CS-7 Recalled by Konica Minolta Medical Imaging USA, Inc. Due to Panasonic...

The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: ImagePilot Recalled by Konica Minolta Medical Imaging USA, Inc. Due to...

The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: There is a potential for imprecise results when using the slides. Increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...

The Issue: Stryker Sustainability Solutions has received an increase in reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Human Design Medical Llc

Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...

The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.

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

Class III — Low RiskOngoing
Medical DeviceMay 8, 2018· Wescam Inc

Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...

The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Zeiss, Carl Inc

Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...

The Issue: In certain eyepiece configurations the laser shutter may not close...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm identified four US lots of test strips out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...

The Issue: Potential for positively biased results

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Thermo Fisher

Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...

The Issue: Product may fail performance testing for S aureus ATCC 43300.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Synthes (USA) Products LLC

Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...

The Issue: The adapter may demonstrate a degradation of function as the final products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Vascular Solutions, Inc.

Recalled Item: Drainer(R) Centesis Catheters: (a) Recalled by Vascular Solutions, Inc. Due...

The Issue: The supplier of Drainer(R) centesis catheters notified Vascular Solutions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing