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. 2,531 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,531 in last 12 months

Showing 97019720 of 48,219 recalls

Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml Recalled by...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Recalled...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-PRO 2 . Intended as an ambulance cot to transport Recalled by Stryker...

The Issue: Transport Cot has insufficient volume of epoxy to assemblies installed in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine II Insulin Syringe 0.5mL Recalled by Becton Dickinson &...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - Recalled by...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Scientia Vascular, Inc.

Recalled Item: Plato 17 Microcatheter: Straight Tip Recalled by Scientia Vascular, Inc. Due...

The Issue: Microcatheters for embolic coil and diagnostic agent introduction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml Recalled by Becton...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - Recalled by BioFire...

The Issue: Due to temperature excursions with products (products being stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1)...

The Issue: Due to temperature excursions with products (products being stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml Recalled by...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - Recalled by BioFire...

The Issue: Due to temperature excursions with products (products being stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Recalled...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Preat Corp

Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...

The Issue: Product is labeled with an incorrect expiration date.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2023· Aniara Diagnostica LLC

Recalled Item: BIOPHEN Protein C 5 kit is for in vitro quantitative Recalled by Aniara...

The Issue: New warnings and precautionary statements on product labelling: Reagent 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...

The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...

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

Class II — Potential Health HazardOngoing
DrugJanuary 31, 2023· BIOCON PHARMA INC

Recalled Item: Posaconazole Delayed-Release Tablets Recalled by BIOCON PHARMA INC Due to...

The Issue: Failed Impurities/Degradation Specifications: High Out Of Specification...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 31, 2023· TWO RIVERS COFFEE LLC

Recalled Item: Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection packaged Recalled...

The Issue: Coffee pods may contain undeclared peanut residue

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

Class III — Low RiskOngoing
Refund