State
73,833 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Misty Mate is recalling about 9,000 hand-held personal misters sold at Hibbet Sports because the plastic cylinder can shatter, posing a laceration risk.
Seagrave is recalling 2013-2014 emergency vehicles because seat belt buckles may fail to release, hindering egress during emergencies.
Avon is recalling Ergonomic Eyelash Curlers because they can break and expose a metal pin, posing an eye injury hazard.
Paramount is recalling Trident Series 2 UV pool sanitizers because electrical arcing can cause the units to catch fire. Consumers should unplug the units and contact the manufacturer for a free replacement.
Pierce Manufacturing is recalling 150 model year 2013 vehicles because seat belt buckles may fail to release, potentially hindering emergency egress.
Coleman is recalling Northstar liquid fuel lanterns because an incorrect gas feed tube can cause fuel leaks, posing fire and burn risks.
General Motors is recalling 2014 Buick Lacrosse and Chevrolet Malibu vehicles because incorrect front brake rotors may cause brake pad detachment and reduced braking.
Turtle Top is recalling 2013 Odyssey and Van Terra buses because wheelchair lift cables may cause a short circuit and fire.
Thermo King is recalling specific truck refrigeration units because plastic side panels may detach in wind, creating road hazards.
Classic Concepts is recalling Aman Trunks sold at Cost Plus World Market because the interior metal chains contain excessive lead, violating federal standards.
Deseo Rebajar is recalling Adipotrim XT dietary supplements because FDA testing found undeclared fluoxetine and the product was marketed without an approved NDA/ANDA.
Baxter Healthcare is recalling 27,169 containers of Dianeal Low Calcium with Dextrose peritoneal dialysis solution due to reported leaks and mold contamination.
B. Braun Medical Inc. is recalling TrophAmine (10% Amino Acid Injection) units due to visible particulate matter found in reserve samples.
B. Braun Medical Inc. is recalling Cefazolin Sodium injectable products because visible particulate matter was found in reserve sample units.
Medisca Inc. is recalling specific lots of Human Chorionic Gonadotropin (HCG) because the labels contain erroneous potency information.
B. Braun Medical Inc. is recalling Ceftriaxone for Injection and Dextrose Injection due to visible particulate matter found in reserve sample units.
B. Braun Medical Inc. is recalling 0.9% Sodium Chloride Injection USP due to visible particulate matter found in reserve sample units.
B. Braun Medical Inc. is recalling Cefoxitin and Dextrose injectable products due to visible particulate matter found in reserve sample units.
B. Braun Medical Inc. is recalling ProcalAmine injectable products due to visible particulate matter found in reserve samples.
B. Braun Medical Inc. is recalling 6.9% FreAmine HBC (Amino Acid Injection) units due to visible particulate matter found in reserve samples.
B. Braun Medical Inc. is recalling Cefepime Hydrochloride and Dextrose injection units because visible particulate matter was found in reserve samples.
Hospira Inc. is recalling Lidocaine Hydrochloride Injection due to confirmed particulate matter in the glass containers.
Hospira is recalling 13,218 Abbott Acclaim Infusion Pumps because broken door assemblies may prevent the door from closing, potentially causing unrestricted flow or therapy delays.
Chrysler is recalling 2013-2014 Fiat 500e vehicles because a coolant leak in the power inverter module may cause a short circuit, leading to loss of propulsion and increased crash risk.
Hospira is recalling 13,218 Acclaim Encore infusion pumps because broken door assemblies may prevent proper closure, causing unrestricted flow or therapy delays.