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. 2,273 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,273 in last 12 months

Showing 4274142760 of 47,632 recalls

Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture Recalled by Smith & Nephew, Inc....

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture Recalled...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Quick Thin (citrus aurantium extract Recalled by Bethel Nutritional...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel Advance (bitter orange Recalled by Bethel Nutritional Consulting, Inc...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...

The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Medicel Ag

Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...

The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2013· American Health Packaging

Recalled Item: Valacyclovir HCl Tablets Recalled by American Health Packaging Due to Subpotent

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ranitidine Hydrochloride Tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Microbial Contamination of Non-Sterile Products: A lot of raw material used...

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

Class II — Potential Health HazardOngoing
Refund