State

Northern Mariana Islands product recalls

73,741 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 23
Critical: 0
Severe: 18
Most recent: 2026-09-23

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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39926–39950 of 73764

HighFDA (Devices)·Z-0498-2018·2018-02-07
Roche Recalls cobas e 411 Analyzers Due to Software Malfunction
Roche Diagnostics is recalling 923 cobas e 411 Immunoassay Analyzers because a software malfunction may cause data mismatches in sample and control files.
Product
cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number: 04775279001/04775279973 - cobas e 411 analyzer (disk system) and 04775201001/04775201973 - cobas e 411 analyzer (rack system), medial device listing number: E116019 cobas e 411 Elecsys analyzer is a fully automated…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0424-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0443-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted during rework, potentially preventing proper product assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 300MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0464-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 300MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0437-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 420MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent the set screw and sleeve assembly from staying in place.
Product
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 340MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0503-2018·2018-02-07
Beaver Xstar Safety Crescent Blades Recalled Due to Exposed Blade
Beaver-Visitec is recalling 123,240 units of Xstar Safety Crescent blades because the protective shield retracted, exposing the blade.
Product
bvi Beaver Xstar Safety Crescent, 2.5mm, 55o Bevel Up, REF 378234 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0481-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 380MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0475-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 13MM X 460MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0245-2018·2018-02-07
Neutrogena Holiday Trays Recalled for Container Leakage
Johnson & Johnson is recalling Neutrogena Elevated 4-Holiday Trays due to defective containers that leak propellant and product.
Product
Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean Purifying Whipped Foam Cleanser) Case Code: 00070501302866
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0310-2018·2018-02-07
Medline Suture Removal Tray Recalled for Subpotent Iodine Content
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
Product
Medline Suture Removal Tray, Sterile, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Mundelein, IL 60060
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0422-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, 130 DEG 11MM X 180MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0249-2018·2018-02-07
Taro Recalls Clobetasol Propionate Cream Due to Content Uniformity Failure
Taro Pharmaceuticals is recalling 27,792 tubes of Clobetasol Propionate Cream 0.05% because the product failed content uniformity specifications.
Product
CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0496-2018·2018-02-07
Edwards HemoSphere System Recalled for Pre-Procedural Software Defects
Edwards Lifesciences is recalling 198 HemoSphere System devices due to pre-procedural software defects. The devices are distributed in 11 US states.
Product
Hemosphere System with the following three components: HEM1 Advanced Monitor, HEMSGM10 (Swan-Ganz Module), and HEMOXSC100 (Oximetry Smart Cable). Product Usage: The HemoSphere Advanced Monitor (HEM1) is intended to be used in combination with a compatible Edwards…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0305-2018·2018-02-07
Medline Incision Drainage Kit Recalled for Subpotent Iodine Content
Medline is recalling Incision Drainage Kits because the iodine content is below the labeled claim. The product was distributed nationwide and internationally.
Product
Medline Incision Drainage Kit, Sterile, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Mundelein, IL 60060
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0421-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of Affixus Hip Fracture Nails because set screws and sleeves may have shifted during rework, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, 125 DEG 9MM X 180MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0444-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 340MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0315-2018·2018-02-07
Medline Incision Drainage Tray Recalled for Subpotent Iodine Concentration
Medline Industries is recalling specific lots of Incision Drainage Trays because the iodine concentration is below the label claim.
Product
Medline Incision Drainage Tray, Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0284-2018·2018-02-07
Medline Suture Removal Tray Recalled for Subpotent Iodine Concentration
Medline Industries is recalling Suture Removal Trays because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
Product
Medline Suture Removal Tray, Sterile, Single Use Only. Packaged in USA for Medline Industries, Inc., Mundelein, IL 60060
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0471-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of the Affixus Hip Fracture Nail because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0341-2018·2018-02-07
PD-Rx Recalls Ibuprofen 200 mg Tablets Due to Manufacturing Deviations
PD-Rx Pharmaceuticals is voluntarily recalling 7,174 bottles of Ibuprofen 200 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC 55289-673-30; c) 50 tablets NDC 55289-673-50; d) 60 tablets NDC 55289-673-60
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0253-2018·2018-02-07
Medline IV Circulation Pack Recalled for Subpotent Iodine Prep Pads
Medline is recalling IV Circulation Packs because the iodine prep pads contain less iodine than labeled. The product was distributed in the US and 10 other countries.
Product
Medline CC Drawer 4 IV Circulation Pack, Contains Rx, Single Use Only, contains 2 Prep Pad PVPs. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0242-2018·2018-02-07
Boehringer Ingelheim Recalls SPIRIVA HandiHaler Due to Failed Stability Specifications
Boehringer Ingelheim is recalling SPIRIVA HandiHaler (tiotropium bromide) capsules because they failed stability specifications. The recall affects 45,008 units distributed nationwide.
Product
SPIRIVA — SPIRIVA (TIOTROPIUM BROMIDE)
Category
Drug
Distribution
Distributed nationwide