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. 2,535 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,535 in last 12 months

Showing 77617780 of 48,219 recalls

DrugAugust 15, 2023· TMC Acquisitions LLC dba Tailor Made Compounding

Recalled Item: Semaglutide/Cyanocobalamin 2mg/0.4mg/mL Recalled by TMC Acquisitions LLC dba...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2023· TMC Acquisitions LLC dba Tailor Made Compounding

Recalled Item: NAD+ 200mg/ml Recalled by TMC Acquisitions LLC dba Tailor Made Compounding...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 15, 2023· Inmar Supply Chain Solutions, LLC

Recalled Item: Multiple FDA-regulated products. Pallets Recalled by Inmar Supply Chain...

The Issue: Potential exposure to rodents and rodent activity in the warehouse.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2023· Caplin Steriles Limited

Recalled Item: Milrinone Lactate Injection Recalled by Caplin Steriles Limited Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 14, 2023· Baxter Healthcare Corporation

Recalled Item: Bendamustine HCl Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Labeling: Missing Label; customer complaint received that labels were...

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

Class III — Low RiskOngoing
Refund
DrugAugust 14, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180...

The Issue: Subpotent: Out of Specification for Assay Test at the 3-month time point.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 14, 2023· Remel, Inc

Recalled Item: remel TODD HEWITT W. CNA (LIM BROTH) Recalled by Remel, Inc Due to On lot of...

The Issue: On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2023· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to One lot of KWIK STIK ANA (3...

The Issue: One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains,...

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

Class III — Low RiskOngoing
DrugAugust 11, 2023· Baxter Healthcare Corporation

Recalled Item: Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Lack of Assurance of Sterility: Potential presence of leaks originating from...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 11, 2023· Baxter Healthcare Corporation

Recalled Item: DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution 1.5% Dextrose...

The Issue: Lack of Assurance of Sterility: Potential presence of leaks originating from...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2023· Imprimis NJOF, LLC

Recalled Item: Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075% Recalled...

The Issue: Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0%...

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

Class III — Low RiskOngoing
Refund
DrugAugust 10, 2023· Colgate Palmolive Company

Recalled Item: hello wild strawberry fluoride toothpaste Recalled by Colgate Palmolive...

The Issue: Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz Recalled by...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Letras con Tomate Tomato Based Alphabet Pasta Soup Mix Recalled by...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix Recalled by...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software update corrected an issue where "low" and "terminal" battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing