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. 2,364 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,364 in last 12 months

Showing 3136131380 of 48,219 recalls

DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid Recalled by...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Diocto Syrup (docusate sodium) Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Sennazon (sennosides) Syrup Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Aller-Chlor (chlorpheniramine maleate) Syrup Recalled by Pharmatech LLC Due...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America 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
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...

The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...

The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...

The Issue: "We have received reports of patients hair being caught in the e.cam and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Terumo Medical Corp

Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...

The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...

The Issue: Presence of particulate matter: Confirmed customer report for the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 4, 2016· Genzyme Corporation / Genzyme Biosurgery

Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Amerisource Health Services

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed dissolution specifications - the out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 3, 2016· Golden State Medical Supply Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Golden State...

The Issue: Failed Dissolution Specifications: Out-of-specification results in retained...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2016· Golden State Medical Supply Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Golden State...

The Issue: Failed Dissolution Specifications: Out-of-specification results in retained...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets Recalled by Zydus...

The Issue: Failed Dissolution Specifications: Product did not meet dissolution...

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

Class III — Low RiskOngoing
Refund