The Recall Desk

State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47926–47950 of 73840

  • ModerateFDA (Devices)·Z-2094-2016·2016-07-06

    Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect

    Smith & Nephew is recalling 10 units of Legion HK Femoral Assemblies because the internal cement surface is below specification.

    Product
    LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 5 LEFT, A/P 62 MM, M/L 70 MM, REF 71421375 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1060-2016·2016-07-06

    Actavis Recalls Ciprofloxacin Ophthalmic Solution Due to Impurity

    Actavis Pharma Inc. is voluntarily recalling Ciprofloxacin Ophthalmic Solution due to out-of-specification results for an unknown impurity near expiration.

    Product
    Ciprofloxacin Ophthalmic Solution (0.3% as base), Sterile, Rx only, a) 2.5 mL Bottle, b) 5 mL Bottle, c) 10 mL Bottle, For Topical Ophthalmic Use Only, Hi-Tech Pharmacal Co. Inc., Amityville, NY 11701, NDC: a) 50383-0282-02, b) 50383-282-05, c) 50383-0282-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2099-2016·2016-07-06

    Dako HER2 CISH pharmDx Kit Recalled for Incorrect Probe Concentration

    Dako North America Inc. is recalling 31 kits of the HER2 CISH pharmDx Kit because the HER2 probe concentration was too low.

    Product
    Dako HER2 CISH pharmDx Kit, product code: SK 109 Product Usage: For in vitro diagnostic use. HER2 CISH pharmDx Kit is intended for dualcolor chromogenic visualization of signals achieved with directly labeled in situ hybridization probes targeting the HER2 gene and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2118-2016·2016-07-06

    Philips Ingenuity Core 128 CT Scanner Recalled for Image Artifacts

    Philips is recalling 19 Ingenuity Core 128 CT scanners because software version 3.5.4 may cause swirl-like artifacts on images, potentially requiring patient rescans.

    Product
    Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The Ingenuity Core 128 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2095-2016·2016-07-06

    Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect

    Smith & Nephew is recalling 97 units of the Legion HK Femoral Assembly because the internal surface is below specification, potentially affecting cement adhesion.

    Product
    LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 5 RIGHT, A/P 62 MM, M/L 70 MM, REF 71421365 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2057-2016·2016-07-06

    Dynarex Recalls Specimen Containers Due to Incorrect Sterile Labeling

    Dynarex Corporation is recalling non-sterile specimen containers that were mistakenly packed in cartons labeled as sterile. The recall covers specific lots distributed in the US and Canada.

    Product
    dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product Usage:containers for sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2091-2016·2016-07-06

    Smith & Nephew Recalls Legion Hinge Knee Femoral Assemblies

    Smith & Nephew is recalling Legion Hinge Knee femoral assemblies because the cement application surface is below specification.

    Product
    LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 3 RIGHT, A/P 54.5 MM, M/L 62 MM, REF 71421363 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2117-2016·2016-07-06

    Philips Ingenuity Core CT Systems Recalled for Image Artifacts

    Philips is recalling 18 Ingenuity Core CT systems because software version 3.5.4 may cause swirl-like artifacts on images, potentially requiring patient rescans.

    Product
    Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity Core scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2084-2016·2016-07-06

    Integra LifeSciences Recalls METASURG Capture Screw System K-wires

    Integra LifeSciences is recalling 182 K-wires used in the METASURG Capture Screw System because they do not meet material, surface, and dimensional specifications.

    Product
    K-wire, Smooth Double-pointed 0.8 x 90mm, a component of the METASURG Capture Screw System The K-wire is used in conjunction with the 2.0 mm cannulated screws for the METASURG Capture Screw System. The K-wire is used by the physician to insert into the bone and to act as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2116-2016·2016-07-06

    Philips Brilliance 64 CT Scanner Recall for Image Artifacts

    Philips is recalling 94 Brilliance 64 CT scanners due to intermittent swirl-like ring artifacts on images, which may require patient rescans.

    Product
    Brilliance 64, Computed Tomography X-ray system Product Usage: The Brilliance CT 64 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1052-2016·2016-07-06

    Lupin Recalls Lisinopril and Hydrochlorothiazide Tablets Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling specific lots of Lisinopril and Hydrochlorothiazide tablets because they were manufactured using active ingredients that failed specifications.

    Product
    LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1053-2016·2016-07-06

    Aloe Source Recalls Topical Analgesic Products Due to Manufacturing Deviations

    The Aloe Source is voluntarily recalling specific lots of aloe SPORT liniment and eucalyptus cream due to CGMP deviations.

    Product
    aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube, ALOE VERA Liniment Topical Analgesic 8 fl oz. bottle, Manufactured by Coats International, Inc., the ALOE SOURCE SPORT Sport Thermogenic Eucalyptus Cream 1 fl oz. plastic bottle, Dallas, TX 75243, NDC 58826-704-08, UPC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1061-2016·2016-07-06

    Aidarex Recalls Ciprofloxacin Ophthalmic Solution Due to Unknown Impurity

    Aidarex Pharmaceuticals is recalling 599 bottles of Ciprofloxacin Ophthalmic Solution because testing revealed out-of-specification results for an unknown impurity.

    Product
    Ciprofloxacin OPTH 0.3% SOL, generic for: Ciloxan, Rx Only, 2.5 mL Bottle, Repackaged by: Aidarex Pharmaceuticals, MFG: Hi-Tech Pharmacal Co., Inc., Amityville, NY, 11701, NDC a) 33261-0910-01, b) 33261-0614-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1057-2016·2016-07-06

    KVK-Tech Recalls Benzphetamine Hydrochloride Tablets Due to Cosmetic Scuffing

    KVK-Tech, Inc. is recalling specific lots of Benzphetamine Hydrochloride Tablets due to cosmetic scuffing marks on the tablets.

    Product
    Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1059-2016·2016-07-06

    Valeant Recalls Secobarbital Sodium Capsules Due to Missing Anaphylaxis Warning

    Valeant Pharmaceuticals is recalling 958 bottles of SECONAL SODIUM capsules because the package insert is missing a warning regarding anaphylaxis.

    Product
    SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2051-2016·2016-07-06

    Cardiovascular Systems Recalls ViperWire Advance Peripheral Guide Wire Due to Missing Date

    Cardiovascular Systems Inc is recalling ViperWire Advance Peripheral Guide Wire because the pouch label was missing the use-by date.

    Product
    ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box. For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1058-2016·2016-07-06

    CVS Acid Controller Tablets Recalled for Impurity Specification Failure

    Dr. Reddy's is recalling CVS pharmacy Acid Controller tablets because stability testing revealed an out-of-specification impurity.

    Product
    CVS pharmacy Original Strength Acid Controller tablets, 10 mg, 30-count bottle, OTC, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 150049523
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V507000·2016-07-05

    GM Recalls 2009-2010 Chevrolet Impala for Passenger Air Bag Wiring Defect

    General Motors is recalling 2009-2010 Chevrolet Impalas because the front passenger seat frame may damage sensor wires, potentially disabling air bags or seat belt pretensioners in a crash.

    Product
    CHEVROLET — CHEVROLET IMPALA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V503000·2016-07-05

    Utility Recalls 2014-2016 Trailers Due to Spring Brake Valve Defect

    Utility Trailer Manufacturing Company is recalling 2014-2016 flatbed, refrigerated, and dry van trailers because improperly machined spring brake valves may delay braking, increasing crash risk.

    Product
    UTILITY — UTILITY FLATBED TRAILERS, REFRIGERATED TRAILERS, DRY VAN TRAILERS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V505000·2016-07-05

    VT Hackney Recalls Kidron and Hackney Trailers Due to Brake Defect

    VT Hackney is recalling 2014-2016 Kidron and Hackney trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    KIDRON — KIDRON, HACKNEY REFRIGERATED TRAILER, BEVERAGE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V506000·2016-07-05

    East Manufacturing Recalls 2014-2016 Trailers Due to Brake Valve Defect

    East Manufacturing is recalling 290 model year 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    EAST — EAST FLATBED, FLATBED TIPPER, FRAME DUMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V502000·2016-07-05

    GM Recalls Vehicles for Ignition Key Removal and Rollaway Risk

    General Motors is recalling specific Buick, Chevrolet, and GMC vehicles because the ignition key may be removed without the transmission in Park, creating a rollaway hazard.

    Product
    CHEVROLET — CHEVROLET, BUICK, GMC EQUINOX, REGAL, CRUZE, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16C006000·2016-07-05

    Combi Coccoro Convertible Child Restraints Recalled for Crash Injury Risk

    Combi is recalling Coccoro Convertible Child Restraints because excessive force may be transmitted to the occupant in a crash if the seat is forward-facing and secured only with a lap belt.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V501000·2016-07-05

    Newmar Recalls Motorhomes Due to Exhaust Tube Fire Risk

    Newmar is recalling specific model year 1998-2015 motorhomes because a flexible exhaust tube may tear, allowing hot exhaust to contact other components and increase the risk of a fire.

    Product
    NEWMAR — NEWMAR KOUNTRY STAR, VENTANA, DUTCH STAR, ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide