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.
Waterway Plastics is recalling Designer Pro Series suction covers installed in select spas due to a risk of entrapment. No injuries have been reported.
DeRoyal Industries is recalling 5,112 units of SafeLiner Suction Canister Kits due to an insufficient seal under low or intermittent suction conditions.
Mortara Instrument is recalling 624 Surveyor S12 and S19 patient monitors due to a potential safety hazard when mounted with non-standard screws.
Boston Scientific is recalling COGNIS CRT-Ds and TELIGENT ICDs due to a capacitor defect that may cause the battery to deplete prematurely.
Boston Scientific is recalling TELIGEN ICDs and COGNIS CRT-Ds due to a capacitor defect that may cause the battery to deplete prematurely.
Codman & Shurtleff is recalling 93,558 EDS 3 Drainage Systems because tubing may leak or disconnect, risking improper fluid drainage or air introduction.
Zimmer, Inc. is recalling 618 units of the Persona Tibial Articular Surface Inserter because they did not undergo heat treatment, creating a risk of tip deformation.
DeRoyal Industries is recalling 13,900 non-sterile suction canisters and lids because they may have an insufficient seal under low or intermittent suction conditions.
Cane Creek is recalling DBINLINE rear shocks because incorrect graphics mislead riders on adjustment directions, posing a fall hazard.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur HBc Total reagents due to increased imprecision and positive bias that may cause false reactive results.
Siemens is recalling ADVIA Centaur HBc Total kits due to increased imprecision and positive bias that may cause false reactive results.
Plum, Inc. is recalling Little Cremes rice milk snacks because they are not softening as intended, posing a choking hazard to babies and young children.
Plum, Inc. is recalling Little Cremes organic rice milk snacks because they are not softening as intended, posing a choking hazard to babies and young children.
Philips is recalling Avalon fetal monitors with specific software because automatic blood pressure measurements stop in certain modes.
Philips is recalling IntelliVue monitors with specific software revisions because the automatic blood pressure measurement series stops in time-synchronized mode.
Zimmer, Inc. is recalling 19 Continuum Acetabular System hip prosthesis shells because they are missing polar boss threads.
Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.
Plum, Inc. is recalling Little Cremes organic rice milk snacks because they are not softening as intended, posing a choking hazard to babies and young children.
Hospira Inc. is recalling 145,600 vials of Hydromorphone Hydrochloride Injection because customer complaints confirmed that some glass vials may be broken or cracked, compromising sterility.
Ad-Tech Medical Instrument Corporation is recalling Cueva Electrode Kits because the applicator wand may malfunction, potentially preventing monitoring of the VII cranial nerve.
Aerogen is recalling 323 FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover broke and dislodged from the adapter body.
Michael Foods is recalling Papetti's Table Ready Refrigerated pre-cooked scrambled eggs because the product may be contaminated with a spoilage microorganism.
Michael Foods is recalling Papetti's Table Ready scrambled eggs due to potential contamination with a spoilage microorganism. The product was distributed nationwide.
Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.
Signal Medical Corporation is recalling 41 Symmetric Total Knee Femoral Components because their packaging was compromised. The components were distributed in Missouri and Panama.