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. 2,503 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,503 in last 12 months

Showing 1498115000 of 27,462 recalls

Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CKMB Calibrator 2-pack Japan Recalled by Siemens Healthcare...

The Issue: A potential bias was identified with certain kits compared to the internal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM CKMB Master Curve Material Recalled by Siemens Healthcare...

The Issue: A potential bias was identified with certain kits compared to the internal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Qiagen Sciences LLC

Recalled Item: EZ1 Advanced XL Recalled by Qiagen Sciences LLC Due to An issue with the...

The Issue: An issue with the power branching printed circuit board (PCB) on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Tecan US, Inc.

Recalled Item: Freedom EV0-2 with any version of EVOware and EVOware Sample Recalled by...

The Issue: There is a software issue that can potentially impact sample identification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Polyisoprene Condoms Recalled by Reckitt Benckiser LLC Due...

The Issue: The products failed the filed specification of 1.0kPa for Burst Pressure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Johnson & Johnson Vision Care, Inc.

Recalled Item: Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear Recalled by...

The Issue: Johnson and Johnson Vision Care received a number of reports of a partially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: EC20CS EPIDURAL CATHETER Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFSDTD EPID TRAY W/17GA FIXED WING Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CNB200TKU NON-STIM CATH FULL KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CNBFX350O CONTIPLEX CONT NERVE BLOCK Recalled by B. Braun Medical, Inc. Due...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKPS CONTINUOUS EPIDURAL ANES TRAY Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKCD CONT EPIDURAL ANESTHESIA KIT Recalled by B. Braun Medical, Inc. Due...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: EPID PAED FULL KIT 24GA CT NG CATH LF Recalled by B. Braun Medical, Inc. Due...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CONTIPLEX TUOHY ULTRA 2 IN CONT. PNB SET Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFCS CONT EPID TRAY W/17G TUOHY-LF Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18TKCD CONT EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18TBLS CONT EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CONTIPLEX TUOHY SET Recalled by B. Braun Medical, Inc. Due to The catheter...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18TKPS CONT EPIDURAL TRAY (LF) Recalled by B. Braun Medical, Inc. Due to...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing