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. 2,357 recalls have been distributed to Wyoming in the last 12 months.
Showing 33521–33540 of 48,219 recalls
Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...
The Issue: OraSure Technologies, Inc. discovered the package insert included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for...
The Issue: Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jadak Barcode Scanner Recalled by CareFusion 303, Inc. Due to Customers...
The Issue: Customers reported issues when scanning medications with the scanners. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17...
The Issue: Hain Celestial Seasoning is recalling Celestial Seasonings Roastaroma Herbal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Buck's Fish Batter Mix Original Recalled by BlendTech Inc Due to...
The Issue: Product contains an undeclared milk ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BCS XP Automated Blood Coagulation Analyzer System Recalled by Siemens...
The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000¿ is...
The Issue: When a user performed radiography using the wireless FPD, a message window...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS Automated Blood Coagulation Analyzer System Recalled by Siemens...
The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: risperiDONE ORALLY DISINTEGRATING TABLETS Recalled by Zydus Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista LOCI Estradiol Test Code E2 Catalog Number: K6463 Recalled...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number:...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF...
The Issue: The Firm has discovered a Software bug.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 Recalled by Resmed Corporation Due to Resmed Corporation is...
The Issue: Resmed Corporation is recalling Astral 100, 150 External Battery because of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Estradiol Test Code E2 Catalog Number: LKE21 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 EstradiolTest Code E2 Catalog Number: L2KE22 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parade Salted Peanuts Dry Roasted Recalled by Star Snacks Co., Llc. Due to...
The Issue: Parade Salted Peanuts Dry Roasted, 8 oz can may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.