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. 1,663 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,663 in last 12 months

Showing 4308143100 of 47,632 recalls

DrugJune 25, 2013· Apotex Inc

Recalled Item: Latanoprost Ophthalmic Solution Recalled by Apotex Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed at expiry for Preservative...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2013· Fresenius Kabi USA, LLC

Recalled Item: Oxytocin Injection Recalled by Fresenius Kabi USA, LLC Due to Subpotent...

The Issue: Subpotent Drug; 15-month stability test station

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2013· Stelkast Co

Recalled Item: SC2316 Recalled by Stelkast Co Due to The firm became aware of an incident...

The Issue: The firm became aware of an incident relating to a breach of sterility in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-852-000 (Console 230V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole)...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: Recalled...

The Issue: A complaint was received of the tips of the Matrix 5.5.mm Left and Right...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 0.5 mL LeGoo with 3 Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Picis Inc.

Recalled Item: Picis ED Pulsecheck - EMR Software Application - 2125 Recalled by Picis Inc....

The Issue: Notes associated with prescription are not printed to the prescription or to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.25 mL LeGoo with 3 Cannula Pouch...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK

Recalled Item: MHI-TM2000 Linear Accelerator System Recalled by MITSUBISHI HEAVY...

The Issue: Software anomaly: Mitsubishi Heavy Industries, Ltd. became aware of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo w/ no Cannula Product...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo with 3 Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder .5mL Product Number: 10-0050 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo with 3 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 1mL Product Number: 10-0100 LeGoo is Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Endovascular Occlusion Gel 2.5 mL Product Number: LG250IT LeGoo...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Endovascular Occlusion Gel 1.0 mL Product Number: LG100IT LeGoo...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo w/ no Cannula Recalled by...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing