State
20,307 recalls have nationwide distribution and so reach North Dakota. 0 additional recalls listed North Dakota specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect North Dakota consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Ampicillin for Injection (500 mg/vial) is being recalled nationwide due to inability to assure sterility. The recall covers approximately 59,530 vials.
Ceftriaxone for Injection is being recalled due to lack of assurance of sterility. The recall affects 65,950 vials distributed nationwide in the United States.
Ampicillin for Injection (2g per vial) is being recalled nationwide because the manufacturer cannot assure the product meets sterility standards. All 45,160 affected vials in circulation are included.
Ampicillin for Injection is being recalled by Xellia Pharmaceuticals because the manufacturer cannot assure the vials are sterile. The nationwide recall involves 220,340 vials.
Philips is recalling 25 CombiDiagnost R90 R1.1 diagnostic imaging systems nationwide due to missing FDA certification labels required for regulatory compliance.
Greiner Bio-One blood collection tubes (VACUETTE TUBE 6ml K3EDTA) may be incorrectly labeled. The company is recalling 36,000 units distributed in Wisconsin and Georgia.
Beckman Coulter is recalling Bicarbonate reagent (REF: OS6637) due to potential calibration failures. The reagent could produce decreased optical density readings affecting laboratory quality control.
3M is recalling 2.2 million Attest Steam Chemical Integrators (REF 1243B) due to an increased potential for ink leakage during sterilization cycles. No injuries have been reported.
Philips is recalling 25 CombiDiagnost R90 diagnostic systems nationwide due to missing required FDA certification labels. Affected healthcare facilities should contact Philips for instructions.
Hiossen Inc. is recalling 287 units of ET III Nano-HA dental implants due to incorrect package labeling stating implant length as 10mm when the actual length is 8.5mm. No illnesses or injuries have been reported.
Philips North America is recalling 25 ProxiDiagnost N90 R.1.0 and CombiDiagnost R90 diagnostic imaging systems distributed nationwide because they are missing an FDA-required certification label.
The CPSC is warning consumers to stop using BQQZHZ combination smoke and carbon monoxide detectors immediately because they can fail to alert to hazardous smoke and fire. About 25,000 units sold on Amazon.com are affected.
About 456,000 PowerXL Stuffed Wafflizer waffle makers are being recalled because hot pieces of waffle or stuffing can be expelled during use or when opening the product, creating a burn risk. The firm has received 44 incident reports, including 34 burn injuries with three requiring medical attention.
Polaris is recalling about 20,330 Model Year 2021–2023 RZR Pro XP 4 and Model Year 2022–2023 RZR Turbo R 4 recreational off-road vehicles because a fuel leak at the fuel pump assembly can occur near a hot surface, posing a fire hazard. The company has received five reports of fuel leaks, including one report of fire.
Target is recalling approximately 4.9 million Threshold Glass Jar Candles because the glass jar can crack or break during use, posing laceration and burn hazards. Six injuries, including lacerations and severe burns, have been reported.
Messingschlager USA LLC (Cycle Force) is recalling about 1,750 Ventura Adult Bike Helmets because they do not meet federal safety standards for positional stability and can fail to protect in a crash. No injuries have been reported.
Acme United is recalling PhysiciansCare Allergy, Allergy Plus, and Cold and Cough tablets sold on Amazon.com from January 2021 through August 2022 because the packaging is not child resistant, risking poisoning if young children swallow the contents.
Shimano is recalling about 400 PRO Vibe Alloy stems for road bicycles because the stems can crack and break during use, causing loss of control and crash risk. Two reports of cracking have been received in the U.S., but no injuries have been reported.
Kell Electronic is recalling about 25,000 Personal Chiller Mini Fridge Gamer Beverage Refrigerators with LED Lights because the power cord can overheat and cause burns. No injuries have been reported.
DKB Household is recalling Cole & Mason 505WEG Pepper Mills due to a metal grinding mechanism that sheds metal shards during initial use, posing a laceration risk. No injuries have been reported.
Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets due to unsecure connections with 15mm caps and circuit components that may disconnect during medical procedures.
Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because the device connectors are not making secure connections with 15mm caps and other circuit components, resulting in unsecure connections.
EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.
Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.
TDHisto/Cyto laboratory management software may display incorrect information on slide labels in specific use cases. The FDA has issued a Class II recall affecting laboratories nationwide in California.