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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 26361–26380 of 27,462 recalls
Recalled Item: Gish 3/8 x 1/2" Reducer Connector with Luer fitting Recalled by Sorin Group...
The Issue: Due to a molding irregularity, certain lots of connectors have the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minotrol 16 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: HORIBA Medical Irvine Technical Support received reports from some customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version...
The Issue: Fluoroscan Mini C-Arm models -InSight2, version 4.0 and 4.0.1 - DICOM images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight2 Recalled by Hologic, Inc....
The Issue: InSight2, version 4.0 and 4.0.1 - DICOM images stored in PACS may be flipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac...
The Issue: 3M determined that the electrical grounding mechanism for the Steri-Vac 5XL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501...
The Issue: Certain Samaritan 300/300P PAD devices may experience one or both of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip System Femoral Stem Petite Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Femoral Stem 12/14 Neck Taper Extended Offset Recalled by Zimmer, Inc....
The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Modular Stem Recalled by Zimmer, Inc. Due to Zimmer Inc. is initiating a...
The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary...
The Issue: A complaint received from sales representative that a replenishment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost with patient carriage Model: 712050 with serial...
The Issue: Hook does not securely hold the footplate in vertical position, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Magnetom Skyra Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: When positioning the Flex Large 4 Coil (part No. 8625761) off-center in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL M4735A Defibrillator/Monitors Recalled by Philips...
The Issue: HeartStart XL Defibrillator/Monitor (M4735A) used on a patient when AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR Assay: Catalog Number: US: Recalled by Siemens...
The Issue: BR Assay for CA 27.29 Calibration Interval Change due quality control (QC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility...
The Issue: The potential exists for the wheel to rotate freely despite engagement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: Recalled...
The Issue: Terumo Cardiovascular Systems (CVS) received two reports of the false back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cemented Tibial Drill Product Usage: The cemented tibial drill is Recalled...
The Issue: Zimmer is initiating a recall of the Cemented Tibial Drill for the Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc Recalled by...
The Issue: The 8 Fr. Bardex All-Silicone Foley Catheter with 3cc balloon had an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set with 150 mL Burette Recalled...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.