State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56426–56450 of 73850

HighFDA (Drugs)·D-0068-2015·2014-11-05
Martin Avenue Pharmacy Recalls Chlorhexidine Gluconate Ophthalmic Solution
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including chlorhexidine gluconate ophthalmic solution, due to quality control issues affecting sterility assurance.
Product
Chlorhexidine gluconate 0.02% opthalmic solution packaged in an opaque squeeze bottle eye dropper, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0063-2015·2014-11-05
Martin Avenue Pharmacy Recalls Benzalkonium Chloride Injection Vials
Martin Avenue Pharmacy is voluntarily recalling benzalkonium chloride water for injection due to quality control issues affecting sterility assurance.
Product
Benzalkonium chloride water for injection packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0140-2015·2014-11-05
Martin Avenue Pharmacy Recalls Compounded Testosterone Cypionate Injection
Martin Avenue Pharmacy is voluntarily recalling compounded Testosterone cypionate 200 mg/mL injections due to quality control observations that present a risk to sterility assurance.
Product
Testosterone cypionate 200 mg/mL injection packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0121-2015·2014-11-05
Martin Avenue Pharmacy Recalls Pilocarpine Eye Drops Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Pilocarpine 0.25% ophthalmic solution due to quality control issues that risk sterility assurance.
Product
Pilocarpine (PF) 0.25% opthalmic solution packaged in an opaque squeeze bottle eye dropper, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0059-2015·2014-11-05
Martin Avenue Pharmacy Recalls Atropine Sulfate Eye Drops for Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Atropine sulfate 0.5% ophthalmic solution due to quality control issues affecting sterility assurance.
Product
Atropine sulfate 0.5% opthalmic solution packaged in a squeeze bottle eye dropper, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0077-2015·2014-11-05
Martin Avenue Pharmacy Recalls Dexamethasone Sodium Phosphate Injectable Vials
Martin Avenue Pharmacy is voluntarily recalling dexamethasone sodium phosphate injectable vials due to quality control issues that risk sterility assurance.
Product
Dexamethasone sodium phosphate 24 mg/mL injectable packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0145-2015·2014-11-05
Martin Avenue Pharmacy Recalls Trimethoprim/Sulfadiazine Injection Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling trimethoprim/sulfadiazine excipient stock solution injections due to quality control issues that risk sterility assurance.
Product
Trimethoprim/sulfadiazine excipient stock solution injection packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0125-2015·2014-11-05
Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including Quad mix 1, due to quality control observations that present a risk to sterility assurance.
Product
Quad mix 1, 12 mg/1 mg/10 mcg/0.15 mg/mL (papaverine, phentolamine mesylate, alprostadil, atropine) injectable packaged in a clear glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0095-2015·2014-11-05
Martin Avenue Pharmacy Recalls Lidocaine 1% Injectable Vials
Martin Avenue Pharmacy is voluntarily recalling Lidocaine 1% injectable vials due to quality control observations that present a risk to sterility assurance.
Product
Lidocaine 1% injectable packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0062-2015·2014-11-05
Martin Avenue Pharmacy Recalls Bacteriostatic Water for Injection
Martin Avenue Pharmacy is voluntarily recalling bacteriostatic water for injection due to quality control issues affecting sterility assurance.
Product
Bacteriostatic water for injection packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0165-2015·2014-11-05
Martin Avenue Pharmacy Recalls Tri-mix Injectable Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Tri-mix T108 injectable vials due to quality control observations that present a risk to sterility assurance.
Product
Tri-mix T108, 30 mg/1.5 mg/25 mcg/mL (papaverine, phentolamine mesylate, alprostadil) injectable packaged in a clear glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0129-2015·2014-11-05
Siemens ADVIA Centaur Calibrator C Recalled for Ferritin Assay Sensitivity Issues
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator C kits due to a realignment issue affecting ferritin assay sensitivity.
Product
ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay on the ADVIA Centaur CP system only. (In-Vitro Diagnostic) Catalog Number: 06567787 (6 pack)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0110-2015·2014-11-05
Martin Avenue Pharmacy Recalls Veterinary Injection Suspension Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling veterinary injection suspensions due to quality control observations that present a risk to sterility assurance.
Product
Peng/proc/strep/chlor/hyos (penicillin G, procaine, streptomycin sulfate, chlorpheniramine maleate, hyoscyamine sulfate) (vet) injection suspension packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0083-2015·2014-11-05
Martin Avenue Pharmacy Recalls Histamine Injectable Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Histamine 0.55 mg/mL injectable vials because quality control observations during an FDA inspection raised concerns about sterility assurance.
Product
Histamine 0.55 mg/mL injectable packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0128-2015·2014-11-05
Siemens Recalls ADVIA Centaur Ferritin Calibrator C Due to Analytical Sensitivity Issues
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Ferritin Calibrator C kits due to realignment issues with specific kit lots. The recall affects 8,263 kits distributed worldwide.
Product
ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin assay on the ADVIA Centaur CP system only. (In-Vitro Diagnostic) Catalog Number: 03439230 (2 pack)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0145-2015·2014-11-05
Parker Eclipse Probe Covers Recalled for Incorrect Expiration Date Labeling
Parker Laboratories is recalling Eclipse Probe Covers due to incorrect expiration dates on inner boxes and plastic bags.
Product
Parker Eclipse Probe Cover, Latex Free, REF 38-01, 10 Eclipse Probe Covers, Size: 2.37/1.75"W x 9.5"L (60/44 mm x 241 mm), Lot #D424, Expiry date 04/2016, Pre-gelled inside with Aquasonic 100 Ultrasound Transmission Gel Product Usage: For use as a protective cover for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0166-2015·2014-11-05
Martin Avenue Pharmacy Recalls Tri-mix T25 Injectable Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Tri-mix T25 injectable vials because quality control observations during an FDA inspection presented a risk to sterility assurance.
Product
Tri-mix T25, 4.413 mg/0.145 mg/1.475 mcg/mL (papaverine, phentolamine mesylate, alprostadil) injectable packaged in a clear glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0153-2015·2014-11-05
Zimmer Dental Recalls Spline Twist Implants Due to Labeling Error
Zimmer Dental is recalling 1,044 Spline Twist Implants because the incorrect diameter size was printed on the inner vial.
Product
Spline Twist Implant, HA 3.25mmD X 15mmL; Part No. 2135. Zimmer Dental Spline implant systems are designed for use in edentulous mandibles or maxillae for attachment of complete denture prostheses for immediate or conventional loading, or as a terminal or intermediary…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0154-2015·2014-11-05
Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Labeling Error
Zimmer Dental is recalling specific Tapered Screw-Vent Implants because the incorrect diameter size was printed on the inner vial.
Product
Tapered Screw-Vent Implant, MTX, 4.1mmD X 10mmL X 3.5mm Platform Part No. TSV4B10 Tapered Screw-Vent Implant, MTX, 4.1mmD X 11.5mmL X 3.5mm Platform Part No. TSV4B11 The Tapered Screw-Vent Implants are designed for use in the maxilla or mandible for immediate loading or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0131-2015·2014-11-05
Abbott Lipase Reagent Recalled for Incorrect Package Insert Parameters
Abbott Laboratories is recalling Lipase Reagent 7D80 because package inserts contain incorrect SmartWash parameters for Triglyceride.
Product
Lipase Reagent, 7D80. Used to measure lipase in human serum on the Architect system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0147-2015·2014-11-05
CooperSurgical Recalls Blunt Hurd Cannula Due to Incorrect Package Insert
CooperSurgical is recalling 90 units of Blunt Hurd Cannula because the wrong package insert was included in the shipping materials.
Product
Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0124-2015·2014-11-05
Cook Medical Recalls Spirotome Soft-Tissue Biopsy Needle Sets
Cook Medical is voluntarily recalling Spirotome Soft-Tissue Biopsy Needle Sets because protective caps may have dislodged inside the packaging.
Product
Spirotome" Soft-Tissue Biopsy Needle Set. The Spirotome Biopsy Needle Set includes a two-part introducer needle that consists of a cutting cannula and a trocar stylet, a helical-tip biopsy needle that has been sized to fit through the lumen of the cutting cannula. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0152-2015·2014-11-05
Elekta Recalls Laksell Gamma Knife Perfexion Units Due to Latch Defect
Elekta is recalling 181 Laksell Gamma Knife Perfexion units because latches may lock before being fully turned, resulting in a poorly locked frame.
Product
Laksell Gamma Knife Perfexion
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0139-2015·2014-11-05
Biosense Webster Recalls ThermoCool SmartTouch Navigation Catheters for Labeling
Biosense Webster is recalling ThermoCool SmartTouch Navigation Catheters to provide additional labeling for safe and effective use.
Product
ThermoCool SmartTouch Navigation Catheters, Catalog No. D132701, D132702, D132703, D132704, D132705, D133601, D133602, D133603.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0134-2015·2014-11-05
Cooper Vision Recalls ProClear Toric Contact Lenses for Axis Defect
Cooper Vision is recalling ProClear Toric contact lenses because routine quality monitoring found that some lots were manufactured with the cylinder axis outside allowable specifications.
Product
ProClear Toric contact lenses are made from a material containing 62% water and 38% omafilcon B, a random copolymer of 2-hydroxyethylmethacrylate and methacrylic acid. The lenses have a tint (VAT Blue 6) which is added to make the lens more visible for handling.
Category
Medical Device
Distribution
Distributed nationwide