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. 2,367 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,367 in last 12 months

Showing 2716127180 of 48,219 recalls

Medical DeviceJuly 18, 2017· Vyaire Medical

Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...

The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 300 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100i Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Product Usage: is a software system designed for treatment...

The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2017· BESTHERBS COFFEE LLC

Recalled Item: New Kopi Jantan Tradisional Natural Herbs Coffee Recalled by BESTHERBS...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 17, 2017· NatureBox, Inc.

Recalled Item: NatureBox Sticks 'n Stones Recalled by NatureBox, Inc. Due to Firm received...

The Issue: Firm received notification that a consumer found a peanut in NatureBox...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 14, 2017· Garden Of Light Inc.

Recalled Item: WOODSTOCK ORGANIC MATCHA VANILLA OATS Recalled by Garden Of Light Inc. Due...

The Issue: Potential for Listeria contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine 40 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg)...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: NORepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: BUPIVacaine HCl 0.125% In 250 mL 0.9% Sodium Chloride Bag Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Phenylephrine HCL in 0.9% Sodium Chloride 10 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Glycopyrrolate Injection Solution Recalled by Cantrell Drug Company Due to...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Neostigmine Methylsulfate Injection Solution 5 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Rocuronium Bromide Injection Solution 5 mL Recalled by Cantrell Drug Company...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund