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 20861–20880 of 27,462 recalls
Recalled Item: 11 Panel Dip Card (OPI 2000) Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMO FISHER 6 DRUG CASSETTE Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart 11 Test Cup Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The system provides the ability to transmit patient data files for storage...
The Issue: Display of SpO2 and Non-Invasive Blood Pressure (NIBP) Measurements May Freeze
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLAIR Endovascular Stent Graft Recalled by Bard Peripheral Vascular Inc Due...
The Issue: Bard Peripheral Vascular (BPV) is recalling the Bard Flair Endovascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...
The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...
The Issue: Complaint investigation concluded that although product quality requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...
The Issue: It was reported that packaging was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-stage and three-stage I.V. poles are shipped as an optional Recalled by...
The Issue: It was identified by a customer complaint that some I.V. poles were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The...
The Issue: The NovoCut Suture Manager device may cut the suture during knot tensioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access CEA Assay Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is recalling the Access CEA reagent packs because they were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspiration Ventilator System Recalled by Event Medical LTD Due to A...
The Issue: A component on the systems power board can fail in a manner which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.