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.
Jaguar is recalling 2013 XJ and XF vehicles because they lack required certification labels specifying weight ratings. This non-compliance could lead to vehicle overloading and increased crash risk.
Terex is recalling 2014 TZ-50 trailer-mounted aerial work platforms because a welding process change may cause cracks in the boom section, risking platform failure.
BMC is recalling Stromer ST1 electric bicycles because the front fork can break, posing a crash and injury hazard to riders.
TJX is recalling Gardeners Eden light-up autumn decorations sold at T.J. Maxx, Marshalls, and HomeGoods due to a fire hazard from exposed wiring.
The Conran Shop is recalling 28 Pondicherry dining tables because the lacquer paint may contain excessive lead levels, violating federal standards.
Mira Health Products Ltd. is recalling B-50 capsules because they contain unapproved steroid ingredients, making them unapproved new drugs.
Mira Health Products Ltd. is recalling Super-DMZ Rx 2.0 Capsules because the product contains an unapproved steroid ingredient and was marketed without FDA approval.
Mira Health Products Ltd. is recalling 5,555 bottles of Metha-Drol Extreme capsules because the product contains an unapproved steroid ingredient.
Hospira is recalling 603,768 bags of 0.9% Sodium Chloride Injection because solution leaked through the port cover, compromising sterility.
Phillips Respironics is recalling 572 Trilogy ventilators worldwide because a defective power management board component may cause loss of therapy.
McKesson Technologies is recalling 10 units of the Anesthesia Care system because patient case data did not match the patient data, including data from another case.
Fresenius Kabi is recalling Heparin Sodium Injection vials because they may contain less active ingredient than labeled.
Shimadzu Medical Systems is recalling 56 mobile X-ray systems because a connecting metal plate may crack, posing a structural safety risk.
Keystone is recalling specific 2014 fifth wheels and travel trailers because insufficient lubrication in the inner wheel bearings may cause the wheel to seize or separate, increasing crash risk.
Zero Motorcycles is recalling specific 2014 FX, S, DS, and SR models because the motor rotor may contact the stator, potentially causing the rear wheel to lock up and increasing crash risk.
Elekta, Inc. is recalling Desktop Pro linear accelerator control software because incorrect values may be entered during calibration procedures.
Hospira Inc. is recalling 115,500 vials of Bupivacaine Hydrochloride injection due to a confirmed report of visible particulate matter embedded in the glass vials.
Fitbit is recalling Force activity-tracking wristbands because the materials can cause skin irritation, rashes, or blistering. Consumers should contact Fitbit for a full refund.
Elekta is recalling Agility software version 3.0 because incorrect values can be entered during calibration procedures for medical linear accelerators.
Elekta is recalling Agility software version 3.1 for linear accelerators because incorrect values could be entered during calibration procedures.
Triple E Recreational Vehicles is recalling 2014 Free Spirit motorhomes because the spare tire carrier obstructs the driver's side taillight, increasing crash risk.
Elekta, Inc. is recalling Integrity Version 1.1 software for linear accelerators because incorrect values can be entered during calibration procedures.
GE Healthcare is recalling Solar 8000M and 8000i patient monitors because the Automatic-View-On-Alarm feature may stop functioning after a specific discharge event.
Carestream Health is recalling Kodak 2200 Intraoral X-Ray Systems because the device arms may break early. This affects 347 units distributed in the US and Canada.
Medical Information Technology, Inc. is recalling MEDITECH Microbiology calculator modules due to a risk of patient results being removed from laboratory and electronic medical record systems.