Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,465 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,465 in last 12 months

Showing 1502115040 of 27,558 recalls

Medical DeviceJuly 24, 2018· Mako Surgical Corporation

Recalled Item: Stryker Mako Vizadisc Knee Procedure Tracking Kit Recalled by Mako Surgical...

The Issue: Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip...

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· 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· 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· 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: 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: CE17TFC CONTINUOUS EPID SET W/17G TUOHY 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: CE17TKST CONT EPID W/SOFT TIP 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: 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: CE17TOD CONT EPIDURAL TRAY LF 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: CE17TO CONT EPIDURAL SET LF 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: CE17TKFPS PERIFIX FX CONT. EPID TRAY-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: CE18TKST CONT EPID W/SOFT TIP 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: EC19C 19G X 100CM CATHETER CLOSED 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: CCE18HK10L 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: CNBFX350C 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: CE18HK ACCU-BLOC PERIFIX KIT 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