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. 2,484 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,484 in last 12 months

Showing 1302113040 of 27,558 recalls

Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 69 mm Item # 195248 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 75 mm Item # 195757 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 71mm Item # 195273 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 65mm Item # 195270 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 73mm Item # 195274 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 79 mm Item # 195276 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 63 mm Item # 195751 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 71 mm Item # 195249 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 71 mm Item # 195755 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP- CR Tibial Tray- Interlok 59mm Item # 195268 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 87 mm Item # 195254 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 87 mm Item # 195760 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 67mm Item # 195271 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 69mm Item # 195272 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· WOM World of Medicine AG

Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...

The Issue: The deficit displayed by the pump can differ from the real deficit, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...

The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...

The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...

The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...

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

Class III — Low RiskOngoing