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. 2,529 recalls have been distributed to Wyoming in the last 12 months.
Showing 11101–11120 of 27,462 recalls
Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 34cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Balloon Catheters (IABs)-MEGA 7.5Fr 40cc IAB Kit P/N:...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 7.5 Fr 40cc...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 40cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE SPECIALIZED ORTHOPEDICS Recalled by Nuvasive Specialized...
The Issue: During explantation, standard removal tools can generate sufficient forces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DABRA RA-308 Excimer Laser Recalled by Ra Medical Systems, Inc. Due to Due...
The Issue: Due to the taller wheel mounting on the laser, the laser may fall over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista High Sensitivity Troponin I (TNIH) Flex reagent...
The Issue: Dimension Vista High Sensitivity Troponin I (TNIH) may exhibit a negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Sensis Vibe Hemo system in combination with the MicroPodTM Recalled...
The Issue: The connector linking the EtCO2 module to the HemoBox may break and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The...
The Issue: The catalog ( REF ) number on the peelable inner labels (patient sticker)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product...
The Issue: Thermo Scientific" Remel" Bordetella pertussis Agglutinating Serum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 Software Version R1.0 and R1.1 Recalled by Philips Medical...
The Issue: Philips has become aware of a software issue, where the kV and mA values are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due...
The Issue: Multiple lots being recalled due to a product design issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.