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. 2,484 recalls have been distributed to Wyoming in the last 12 months.
Showing 16581–16600 of 27,462 recalls
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer....
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Recalled...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier III in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prevent G Safety Winged Blood Collection Set Glide - Rx Recalled by...
The Issue: Complain due to the hub needle came out when the nurse draw the blood and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda(R) Intrathecal Catheter Recalled by Medtronic...
The Issue: There is a possibility that specific lots of catheters that have recently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GastriSail" Gastric Positioning Device Product Usage: The GastriSail gastric...
The Issue: Reports of gastric or esophageal perforation occurring in procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...
The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.