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.
NuVision Pharmacy is recalling 285 vials of HCG (Lyophilized) nationwide due to a lack of sterility assurance identified during an FDA inspection.
The Mentholatum Company is recalling several Rohto eye drop products due to concerns about the quality assurance of sterility controls.
The Mentholatum Company is recalling Rohto eye drops because of concerns about sterility controls. The recall covers nationwide distribution and Puerto Rico.
The Mentholatum Company is recalling several Rohto eye drop products due to concerns about the quality assurance of sterility controls.
DeRoyal Industries is recalling 48 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature and have caused electric shocks.
The Mentholatum Company is recalling Rohto eye drops because of concerns about the quality assurance of sterility controls.
Codman & Shurtleff is recalling 369 Certas Programmable Valves used for hydrocephalus because they may not operate properly.
Codman & Shurtleff, Inc. is recalling 431 Codman Certas Programmable Valves because they may not operate properly. These implantable devices are used to manage hydrocephalus.
Hospira Inc. is recalling 15,258 bags of Aminosyn 3.5% M Sulfite-Free due to a lack of assurance of sterility and potential leakage from the administrative port.
Hospira is recalling 27,780 bags of Heparin Sodium 2000 USP Units per 1000 mL due to a lack of assurance of sterility and potential leakage from the administrative port.
DeRoyal Industries is recalling 121 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.
Synergetics Inc is recalling 96 units of 25ga Endo Illuminator devices because faulty seals on the outer pouch could fail, potentially compromising sterility.
Synergetics is recalling 25ga Aspirating Endo Illuminators because faulty seals on the outer pouch could fail, compromising the sterile status of the ophthalmic devices.
Synergetics Inc. is recalling 36 units of 25ga Awh Chandeliers because faulty seals on the outer pouch could fail, compromising the sterile status of the ophthalmic devices.
Synergetics Inc is recalling 48 units of Stiff 25ga Endo Illuminators because faulty seals on the outer pouch could result in seal failure.
Synergetics Inc. is recalling specific lots of Corona Shielded Wide Field Endo Illuminators because faulty seals on the outer pouch could fail, compromising sterility.
The Lambs Farm, Inc. is recalling Banana Nut Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.
Synergetics Inc. is recalling 233 units of 29ga Oshima Dual Chandeliers because faulty seals on the outer pouch could fail, compromising the sterile status of the devices.
Synergetics Inc is recalling 568 units of 23ga Wide Field Endo Illuminators because faulty seals on the outer pouch could result in seal failure.
Nomad is recalling 2013 Dispatch 14A, 20SS0, and 16AS0 trailers because a door lock defect could jam the deadbolt, trapping occupants inside.
Synergetics Inc is recalling 26 units of 23ga Mid-Field Endo Illuminator devices because faulty seals on the outer pouch could fail, compromising sterility.
Sorin Group is recalling S5/C5 Heart-lung machines and CP5 centrifugal pump systems due to pump speed control knob failures that result in no response.
Sorin Group is recalling 75 CP5 centrifugal pump systems due to reports of pump speed control knob failures that result in no response.
Siemens Medical Solutions is recalling 843 ACUSON SC2000 ultrasound systems because the user interface assembly may become loose and fall off.
Codman & Shurtleff is recalling 1,460 Certas Programmable Valves used for hydrocephalus because they may not operate properly.