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. 2,415 recalls have been distributed to Wyoming in the last 12 months.
Showing 20121–20140 of 27,462 recalls
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: 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: 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: 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: Super Arrow-Flex Percutaneous Sheath Introducer Sets or CL-07635 Recalled by...
The Issue: Arrow has issued a recall for these products due to potential packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 13 consists of all product under product code HWC Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 71 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 40 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 47 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 49 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 26 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 41 consists of all product under product code: KTT Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 69 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 32 consists of all product under product code: HWC Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 9 consists of all product under HRS Recalled by Zimmer Manufacturing...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 50 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 39 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.