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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2220122220 of 27,558 recalls

Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper cardio systems R7.6 Model : 722133 Product Recalled...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Bradshaw Medical Inc.

Recalled Item: Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw...

The Issue: A component failure could cause a situation where the applied torque was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Invacare Corporation

Recalled Item: Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair) Recalled by...

The Issue: The batteries used in the Invacare¿ Pronto¿ Air Personal Transporter models...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Smiths Medical ASD, Inc.

Recalled Item: CADD" Medication Cassette Reservoir Recalled by Smiths Medical ASD, Inc. Due...

The Issue: Smiths Medical has become aware of an issue with specific lots of 50mL CADD"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· GE Healthcare

Recalled Item: GE Healthcare Proteus XR/a with wall stand model number 2260354. Recalled by...

The Issue: Potential breakage of the steel cable which supports the bucky device in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· Penner Mfg Inc

Recalled Item: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1...

The Issue: If the patient sits on either wing, not squarely on the center section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Power supply malfunction complaints related to suboptimal thermal management.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· C.R. Bard, Inc.

Recalled Item: Bard 100% Latex-Free Urinary Drainage Bag with Anti- Chamber and Recalled by...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2015· Elekta, Inc.

Recalled Item: Elekta Precise Treatment Table Recalled by Elekta, Inc. Due to It is...

The Issue: It is possible to position the Treatment Table with errors greater than 5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2015· Medical Components, Inc dba MedComp

Recalled Item: 9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The dual port with catheters was not covered under FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2015· Zimmer, Inc.

Recalled Item: Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis Recalled...

The Issue: An increase in complaints of loosening and radiolucent lines.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· GE Healthcare

Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...

The Issue: Potential failure of the caster mounting hardware, which may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: MediChoice WarmGel Infant Heel Warmer Recalled by CooperSurgical, Inc. Due...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: Fisher Brand Gel Infant Heel Gel Warmers Recalled by CooperSurgical, Inc....

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing