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. 2,510 recalls have been distributed to Wyoming in the last 12 months.
Showing 13401–13420 of 27,462 recalls
Recalled Item: Hudson RCI Sheridan: 1) HVT 6.0 mm Recalled by Teleflex Medical Due to This...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan LTS Recalled by Teleflex Medical Due to This voluntary...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan/HVT: 1) Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...
The Issue: Multiple complaints were received for balloons bursting below the rated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...
The Issue: Multiple complaints were received for balloons bursting below the rated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan: 1) Preformed 6.0 mm Recalled by Teleflex Medical Due to...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...
The Issue: Multiple complaints were received for balloons bursting below the rated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan: 1) Uncuffed 6.0 mm Recalled by Teleflex Medical Due to...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen Recalled...
The Issue: During initial set-up and/or replacement of the dispenser batteries, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various products which were contract sterilized. Recalled by Anewmed...
The Issue: The contract sterilizer did not have adequate packaging data to support the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Line Cutting Electrode 11.5Fr Mono 0 degrees Recalled by Richard Wolf...
The Issue: E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "HEMOGLOBIN A1c CALIBRATORS *** *** 307261/R03 *** S4P5X0 Recalled by Abbott...
The Issue: Calibrator level 2 bottle may have been manufactured incorrectly for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The device is a 25-gauge infusion line that is part Recalled by Dutch...
The Issue: Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alinity ci-series System Control Modules which are configured with...
The Issue: All versions of the Alinity ci-series software may not detect an issue on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG Salivary Testosterone ELISA- IVD for the detection of Testerone Recalled...
The Issue: Salivary assay may observe a higher percentage of samples with 0 pg/ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.