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. 2,475 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,475 in last 12 months

Showing 1442114440 of 48,219 recalls

Medical DeviceJuly 21, 2021· Cardiovascular Systems Inc

Recalled Item: DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM Recalled by...

The Issue: There is a potential mislabeling of the OAD crown sizes: 1.50mm Sold Crown...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2021· Cardiovascular Systems Inc

Recalled Item: STEALTH 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM Recalled by...

The Issue: There is a potential mislabeling of the OAD crown sizes: 1.50mm Sold Crown...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2021· Merit Medical Systems, Inc.

Recalled Item: MERITMEDICAL Prelude Short Sheath Introducer Recalled by Merit Medical...

The Issue: There is a potential that a package sheath contains an incorrect dilator.

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

Class II — Potential Health HazardOngoing
DrugJuly 20, 2021· HIS ENTERPRISE INC

Recalled Item: Miss Slim Recalled by HIS ENTERPRISE INC Due to Marketed without ANDA/NDA...

The Issue: Marketed without ANDA/NDA approval

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 20, 2021· Belmont Instrument Corporation

Recalled Item: CritiCool Recalled by Belmont Instrument Corporation Due to Premature pump...

The Issue: Premature pump failure may lead to the device displaying a HALT 4 error,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Welch Allyn Inc

Recalled Item: Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent...

The Issue: If the device is exposed to fluid ingress and is used before the cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Angiodynamics, Inc.

Recalled Item: Solero Generator US PG Recalled by Angiodynamics, Inc. Due to Specific...

The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· NIHON KOHDEN ORANGEMED, INC

Recalled Item: Nihon Kohden NKV-550 Ventilator Recalled by NIHON KOHDEN ORANGEMED, INC Due...

The Issue: Potential defective gas inlet pressure regulator within ventilator which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Angiodynamics, Inc.

Recalled Item: Solero Generator US PG Recalled by Angiodynamics, Inc. Due to Specific...

The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Angiodynamics, Inc.

Recalled Item: Solero Generator PG Recalled by Angiodynamics, Inc. Due to Specific serial...

The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Angiodynamics, Inc.

Recalled Item: Solero Generator PG Recalled by Angiodynamics, Inc. Due to Specific serial...

The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Ethicon Endo-Surgery Inc

Recalled Item: HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for soft tissue...

The Issue: An internal component may be cracked and become lodged behind the energy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC HD 1000i Shears (20cm Shaft Length)-indicated for soft tissue...

The Issue: An internal component may be cracked and become lodged behind the energy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2021· BioFire Diagnostics, LLC

Recalled Item: FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label:...

The Issue: Due to product complaints received for false negative results (dropouts)...

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2021· Teligent Pharma, Inc.

Recalled Item: Triamcinolone Acetonide Ointment USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Correct Labeled Product Mispack

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine HCl Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specification: Some tablets are shaved

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2021· Teligent Pharma, Inc.

Recalled Item: Econazole Nitrate Cream 1% Recalled by Teligent Pharma, Inc. Due to Correct...

The Issue: Correct Labeled Product Mispack

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 19, 2021· Grimmway Enterprises, Inc. dba Grimmway Farms

Recalled Item: Organic Baby Rainbow Carrots Brand name: O Organics 12 oz. Recalled by...

The Issue: Carrot products may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 19, 2021· Grimmway Enterprises, Inc. dba Grimmway Farms

Recalled Item: Shredded Carrots Brand name: Grimmway Farms 10 oz. (284g) plastic Recalled...

The Issue: Carrot products may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 19, 2021· Grimmway Enterprises, Inc. dba Grimmway Farms

Recalled Item: Organic Baby Peeled Carrots 12/12oz Steam-to-Serve Recalled by Grimmway...

The Issue: Carrot products may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund