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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 27361–27380 of 27,462 recalls
Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...
The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Needle 6.5"...
The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle with...
The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade 6.5 ...
The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPARIN LOCK FLUSH SOLUTION Recalled by App Pharmaceuticals Llc Due to CGMP...
The Issue: CGMP Deviations: Incomplete documentation associated with test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPARIN LOCK FLUSH SOLUTION Recalled by App Pharmaceuticals Llc Due to CGMP...
The Issue: CGMP Deviations: Incomplete documentation associated with test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AperFix Femoral Implant Coring Removal Drill Recalled by Cayenne Medical...
The Issue: A review of product complaints in 2010 identified a trend for the Coring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HC OEC 9900 Elite and GE OEC 9800 Fluoroscopes Recalled by GE OEC Medical...
The Issue: GE OEC recalled certain 9800 Fluoroscope & 9900 Elite Models because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Computed Tomography X-Ray System. These devices are...
The Issue: Philips Healthcare discovered the customer was performing CTDI measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A mobile Recalled by Steris Corporation Due to Customers may be storing...
The Issue: Customers may be storing objects on the base and/or around the column of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Handi-Fil Disposable Syringe Fill Tube is a sterile plastic tube...
The Issue: A report was received from a Japanese distributor regarding a complaint from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoHelix Part #HCS-056-32 3.8MM Cannulated Hex Driver NON STERILE MAT:...
The Issue: The tips of the drivers are breaking while being used to drive the screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT:...
The Issue: The tips of the drivers are breaking while being used to drive the screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Recalled by...
The Issue: These camera systems were manufactured by LMGS and found to fail to comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versafitcup Impacting Ring Model Number: 01.26.10.0133 (46mm) Recalled by...
The Issue: Medacta USA is recalling Versafitcup Impacting Ring because the impaction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiegelberg Brain Pressure Monitoring System Probe 3PN Recalled by...
The Issue: In the vast majority of products specified, a shrinkage of the air chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xoran MiniCAT CT Scanner ID ENT00001 Recalled by Xoran Technologies, Inc....
The Issue: Failure of the gantry to rotate. The complaint alleged that the scanner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The Recalled by...
The Issue: The recall was initiated because Carefusion has confirmed that when the PAS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Application Interfacing Outbound Phlebotomy Point of Care Interface...
The Issue: The recall was initiated because Sunquest Information System has confirmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO 3 V1.05(FG-5400-00). The CARTO 3 V1.05 System is intended Recalled by...
The Issue: The recall was initiated because Biosense Webster has become aware of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.