State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer due to damage that can cause electric shock.
Arrow International is recalling Select Kits and Maximal Barrier Precautions Kits containing BD Posiflush syringes because open seals may compromise sterility.
Bumble Bee Foods is recalling Jalapeno Albacore Tuna pouches due to seal defects that could allow contamination by pathogens.
Spartan Motors is recalling 2010-2015 Gladiator vehicles because the engine cooling fan may break during severe vibration, posing an injury risk if the hood is open.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Primus Medical LLC is recalling 1,726 AC powered adjustable bed frames used in nursing facilities because the head deck actuator bracket may separate from the frame.
Intuitive Surgical is voluntarily correcting labeling and software for the EndoWrist One Vessel Sealer used with the da Vinci Si Surgical System.
Kraft Heinz Foods is voluntarily recalling 7,691 cases of American cheese slices because a supplier failed to store an ingredient at the correct temperature.
Valeant Pharmaceuticals is recalling 34,218 tubes of Hydrocortisone Butyrate Cream 0.1% because the product failed stability testing for potency and preservative levels.
Valeant Pharmaceuticals is recalling 1,663 tubes of Locoid cream because the active ingredient and preservatives were subpotent at the 18-month stability test point.
Roche Diagnostics is recalling Omni Micro-electrodes for the cobas b221 analyzer because default reference values are inconsistent with other instruments and instructions.
Zydus Pharmaceuticals is recalling Topiramate 200 mg tablets because 100 mg tablets were found mixed in the bottles.
Gyma Laboratories of America, Inc. is recalling Clonidine Base Micronized due to lack of good manufacturing practices identified by the Italian Medicines Agency.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a software anomaly that may cause unexpected assay calibration when using specific calibrator kits.
Sagent Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because the products were labeled with incorrect expiration dates.
Gyma Laboratories of America, Inc. is recalling Propranolol HCl due to lack of good manufacturing practices identified by the Italian Medicines Agency.
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems because a software anomaly may cause unexpected assay calibration when using specific calibrator barcode labels.
Gyma Laboratories of America, Inc. is recalling Dipyridamole API due to lack of good manufacturing practices identified by the Italian Medicines Agency.
Avella of Deer Valley, Inc. is recalling 197 vials of Hydroxyprogesterone Caproate 250 mg/mL injectable because crystals were observed in the product.
Baxter Healthcare is recalling 15 L Cycler Drainage Bags because the tube clamp may not fully close, potentially causing leakage.
Stryker is recalling T2 Tibia Nail Insertion Sleeves because some units have a different inner diameter than labeled.
Michael Foods, Inc. is recalling 40,966 cases of shell eggs under six different brand labels due to contamination with Pseudomonas fluorescens.
Gyma Laboratories of America, Inc. is recalling Clonidine HCL chemical product for medicines preparation due to lack of good manufacturing practices.
Valeant Pharmaceuticals is recalling 205,853 bottles of Vasotec (enalapril maleate) tablets because they were packaged with the incorrect version of the package insert.
Valeant Pharmaceuticals is recalling Vaseretic tablets because they were packaged with the incorrect version of the package insert.