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. 2,373 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,373 in last 12 months

Showing 2284122860 of 27,558 recalls

Medical DeviceOctober 6, 2014· Alcon Research, Ltd.

Recalled Item: INFINITI Ultrasound Pack. Catalog Numbers: 8065751716 Recalled by Alcon...

The Issue: The recalling firm received complaints related to leakage from the tubing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7004 Part Number: MRI-04 MRI-Poncho Product Usage: Radio...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7009 Part Number: MRI-09 MRI- Leg Wrap Blanket Recalled by...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7010 Product Usage: Radio frequency shielding blankets and...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7008 Part Number: MRI-08 MRI-Boot Product Usage: Radio...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7005 Part Number: MRI-05 Leg Wrap Product Usage: Recalled by...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7003 Part Number: MRI-03 U (Upper) and MRI-03 Recalled by...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2014· Zimmer, Inc.

Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...

The Issue: Failed to meet established requirements for sterile barrier integrity due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer, Inc.

Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...

The Issue: The affected products are missing polar boss threads.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Medartis, Inc.

Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...

The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Roscoe Medical Inc

Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...

The Issue: The caster may separate completely from the device frame causing injury to user.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...

The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2014· Signal Medical Corporation

Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...

The Issue: Packaging of a device was compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2014· Masimo Corporation

Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...

The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: Certain lots of the reagent cartridges show confirmed positive bias...

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

Class II — Potential Health HazardOngoing