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. 2,348 recalls have been distributed to Wyoming in the last 12 months.
Showing 33861–33880 of 48,219 recalls
Recalled Item: Mavig Monitor Suspension System Recalled by GE Medical Systems, LLC Due to...
The Issue: GE Healthcare has recently become aware of a reported incident in which a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoCoil 3.0T GEM Flex Coil. The 3.0T GEM Flex coil Recalled by NeoCoil, LLC...
The Issue: Potential for higher than specified surface temperatures. Use of 3.0T GEM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...
The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oncentra External Beam - VMAT - Radiation therapy planning system Recalled...
The Issue: When using the option "Tumor Overlap Fraction" in VMAT planning it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuse 1C Colonoscope Recalled by EndoChoice, Inc. Due to The bending section...
The Issue: The bending section of the device may partially separate from the insertion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Recalled...
The Issue: Reprocessed Stryker Pressure Tourniquet Cuffs were mislabeled, including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary...
The Issue: Defective Delivery System: Product may contain leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RadSuite Recalled by Merge Healthcare, Inc. Due to Potential incorrect...
The Issue: Potential incorrect Standardized Uptake Values (SUV) measurements in RadSuite.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X are gamma cameras Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView are gamma cameras Recalled by Philips Medical Systems (Cleveland)...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT & BrightView XCT Upgrade Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC Recalled by...
The Issue: Devices reported to have a smooth texture to the outer surface of the metal,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...
The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...
The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...
The Issue: There were two potential interference conditions identified with the way the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZI XIU TANG BEAUTY FACE & FIGURE Capsules Recalled by Bee Extremely Amazed...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Formula Capsules Recalled by Bee Extremely Amazed LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asset BOLD Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.