Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,531 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,531 in last 12 months

Showing 1030110320 of 47,938 recalls

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
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgipro Monofilament Polypropylene Sutures Product Description CP-535...

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· Integra LifeSciences Corp.

Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...

The Issue: Integra LifeSciences identified that one lot was released with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Tomy International Inc.

Recalled Item: Lamaze Chill Teether Recalled by Tomy International Inc. Due to Affected...

The Issue: Affected lots of the product are being recalled due to potential microbial...

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

Class II — Potential Health HazardOngoing
DrugDecember 1, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Oxcarbazepine Tablets 600mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...

The Issue: Presence of foreign substance

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

Class II — Potential Health HazardOngoing
Refund