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. 2,360 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,360 in last 12 months

Showing 2662126640 of 27,558 recalls

Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Biliary Catheters (Models A47XX and CB0XXXXX): Model Numbers & Description:...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent...

The Issue: Firm has received complaints from customers of "Abnormal Reaction" errors...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: Stryker XIA 3 TORQUE WRENCH Manufactured by: Stryker Recalled by Stryker...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2012· Parks Medical Electronics, Inc

Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...

The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...

The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...

The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· ThyssenKrupp Access Corp

Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...

The Issue: The seat could break as a result of damage resulting from a seat belt being...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Diamedix Corporation

Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...

The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....

The Issue: During the manufacturing of the affected lot a manufacturing error has led...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Orthofix, Inc

Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...

The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Elekta, Inc.

Recalled Item: Precise Digital Accelerator Delivery of radiation to defined target volumes...

The Issue: There have been a small number of instances in hospitals where the joint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Invacare Corporation

Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...

The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2012· Instrumentation Laboratory Co.

Recalled Item: Instrumentation Laboratory ACL TOP 700 LAS PN 0000280030 ACL TOP Recalled by...

The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2012· Instrumentation Laboratory Co.

Recalled Item: Instrumentation Laboratory ACL TOP CTS PN 0000280020 ACL TOP is a bench top...

The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...

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

Class II — Potential Health HazardOngoing