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. 2,512 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,512 in last 12 months

Showing 1020110220 of 47,632 recalls

Medical DeviceDecember 5, 2022· Cardiac Assist, Inc

Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...

The Issue: A software update (v1.1.5) has been developed to address the issue of...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 5, 2022· Young Dental Manufacturing I, LLC

Recalled Item: Denticator PICK-A-DENT Recalled by Young Dental Manufacturing I, LLC Due to...

The Issue: mislabeled product

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

Class III — Low RiskOngoing
Medical DeviceDecember 5, 2022· Elekta, Inc.

Recalled Item: Oncentra Brachy radiation therapy planning system software. Recalled by...

The Issue: A reconstruction error may occur when using the Catheter Bending...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Custom Suture Pack Product Description: US1638 CUSTOM SUTURE PACK US1756...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgidac Uncoated Braided Polyester suture Product Description D-1764K...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Sofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgipro II Monofilament Polypropylene Sutures Product Description Model...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing