State

Northern Mariana Islands product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29626–29650 of 73621

SevereFDA (Drugs)·D-0972-2020·2020-03-11
Axia Pharmaceutical Recalls Methylprednisolone Acetate Injectable Suspension Due to Sterility Concerns
Axia Pharmaceutical is recalling specific lots of Methylprednisolone Acetate Injectable Suspension because the company cannot guarantee the product is sterile.
Product
Methylprednisolone Acetate Injectable Suspension, METHYLPREDNISOLONE ACETATE [10ML] CMC 50 MG/ML INJ SUSP, For IM, IA Use, Shake Well, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0636-1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0989-2020·2020-03-11
Axia Pharmaceutical Recalls Triamcinolone Diacetate Injectable Suspension Due to Sterility Concerns
Axia Pharmaceutical is recalling specific lots of Triamcinolone Diacetate Injectable Suspension because the product lacks assurance of sterility.
Product
Triamcinolone Diacetate Injectable Suspension, TRIAMCINOLONE Diacetate [10ML] CMC 10MG/ML INJ SUSP, For IM, IA Use, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0625-1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0932-2020·2020-03-11
Axia Pharmaceutical Recalls Alprostadil Injection Due to Sterility Concerns
Axia Pharmaceutical is recalling Alprostadil/Papaverine/Phentolamine/Atropine Injection due to a lack of assurance of sterility. The product was distributed nationwide and in Puerto Rico, Barbados, and the Dominican Republic.
Product
Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate/Atropine Sulfate Injection, 18 mcg/1.8mg/0.2mg/0.02mg/mL, For Intracavernosal Use, Freeze, 2.5 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0547-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0944-2020·2020-03-11
Axia Pharmaceutical Recalls Betamethasone Injectable Suspension Due to Sterility Concerns
Axia Pharmaceutical is recalling Betamethasone Acetate/Betamethasone Injectable Suspension due to a lack of assurance of sterility. The product was distributed nationwide and in several territories.
Product
BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [5ML] 7MG/ML INJ SUSP, For IM, IA Use, Shake Well. 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2020·2020-03-11
Recall of Covidien Force TriVerse Electrosurgical Devices Due to Packaging Risk
The FDA is recalling 70,361 units of Covidien Force TriVerse Electrosurgical Devices because sterile packaging may be compromised, increasing the risk of infection.
Product
Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V140000·2020-03-11
Heartland Recalls 2020 Shadow Cruiser Ultra Lite Trailers Due to Label Error
Heartland is recalling 2020 Shadow Cruiser Ultra Lite trailers because certification labels list incorrect GVWR and axle ratings, which could lead to overloading and axle failure.
Product
CRUISER RV — CRUISER RV SHADOW CRUISER ULTRA LITE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0967-2020·2020-03-11
Axia Pharmaceutical Recalls Methylcobalamin Injection Due to Sterility Concerns
Axia Pharmaceutical is recalling specific lots of Methylcobalamin Injection because the product lacks assurance of sterility. The recall covers distribution in the U.S., Puerto Rico, Barbados, and the Dominican Republic.
Product
Methylcobalamin Injection, METHYLCOBALAMIN 1 MG/ML INJECTABLE, For IV, IM, SC Use, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0331-3
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1445-2020·2020-03-11
Stryker Connected OR Cart Recalled Due to Monitor Attachment Defect
Stryker is recalling 12 Connected OR Carts because the monitor may not attach correctly, posing a risk of the monitor falling and injuring users.
Product
Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qty 1, Rx Only, Manufactured for: Stryker, 5900 Optical Court, San Jose, CA 95138, UDI: 07613327462784 - Product Usage: The Connect OR Cart is a mobile, medical-grade cart intended to store and transport components of…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V141000·2020-03-11
Turtle Top Odyssey Recall for Seatbelt Warning Light Defect
Turtle Top is recalling 2019 Odyssey vehicles because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition, increasing crash injury risk.
Product
TURTLE TOP — TURTLE TOP ODYSSEY
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0986-2020·2020-03-11
Recall of Triamcinolone Acetonide/Bupivacaine Injectable Suspension Due to Sterility Concerns
FDA recalls Triamcinolone Acetonide/Bupivacaine Injectable Suspension due to lack of sterility assurance. The drug was distributed nationwide and in Puerto Rico, Barbados, and the Dominican Republic.
Product
Triamcinolone Acetonide/Bupivacaine Hydrochloride Injectable Suspension, TRIAMCINOLONE ACET/BUPIVACAINE HCL [10ML] 40MG/5MG/ML INJ SUSP, For IM, IA Use, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0632-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1421-2020·2020-03-11
Siemens Atellica CH Reaction Ring Segment Recalled for Cuvette Defects
Siemens Healthcare Diagnostics is recalling Atellica CH Reaction Ring Segments because defects may allow water contamination, leading to inaccurate test results.
Product
Atellica CH Reaction Ring Segment, SMN 11099326, UDI 00630414596143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1443-2020·2020-03-11
RespVent Closed Suction System Tracheostomy T-Piece Recall for Connection Defect
Respiratory Therapeutics Group is recalling RespVent Closed Suction System T-Pieces because catheters may not be tightly connected to the thumb port, potentially reducing suction performance.
Product
RespVent Closed Suction System T-Piece Tracheostomy Adult, Diameter: 4.6mm (14F), Length: 30.5cm (12in.), MDI Adapter, Cont. 10 Closed Suction Catheter, Sterile R, RxOnly, Reorder Number: RTG-02300, UDI: 00850108006035 - Product Usage: To be used to aspirate liquids or semi…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1444-2020·2020-03-11
Roche Recalls Elecsys CA 19-9 Reagent Due to Non-Reproducible Results
Roche Diagnostics is recalling 684 units of Elecsys CA 19-9 reagent because non-reproducible elevated results may affect clinical interpretation.
Product
Elecsys CA 19-9, Cat. No. 07027028190 - Product Usage: the product is an immunoassay for monitoring and management of pancreatic cancer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1439-2020·2020-03-11
Vyaire Medical Recalls bellavista 1000 Ventilators Due to Alarm Failures
Vyaire Medical is recalling 116 bellavista 1000 ventilators because they may fail to sound high-priority alarms or respond to touch screen input.
Product
bellavista 1000 ventilator, Catalog number 301.100.030. bellavista is an electronically controlled pneumatic ventilation system with an integrated air compressing system. bellavista uses room air and high-pressure oxygen. Air enters through a fresh gas intake port and is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2020·2020-03-11
Recall of Force TriVerse Electrosurgical Kits Due to Sterility Concerns
Covidien is recalling Force TriVerse Electrosurgical Kits distributed in EMEA due to potential sterile packaging compromise, which may increase infection risk.
Product
Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed in EMEA (Europe, Middle East, and Africa) only. No US distribution. Kits are manufactured in The Netherlands. Item codes BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0984-2020·2020-03-11
Axia Pharmaceutical Recalls Testosterone Cypionate Injection Due to Sterility Concerns
Axia Pharmaceutical is recalling Testosterone Cypionate Injection because the product lacks assurance of sterility. The recall covers specific lots distributed in the U.S., Puerto Rico, Barbados, and the Dominican Republic.
Product
Testosterone Cypionate Injection, TESTOSTERONE CYP IN GRAPESEED OIL [1ML] 200 MG/ML INJECTABLE, For IM Use, 1 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0530-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1409-2020·2020-03-11
Baxter Recalls Revaclear 300 Dialyzers Due to Potential Foreign Matter
Baxter Healthcare is recalling Revaclear 300 Capillary Dialyzers because of the potential presence of particular matter in the header caps of ten lots.
Product
Revaclear Capillary Dialyzer 300, REF Revaclear 300 Product Code 114745L
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1435-2020·2020-03-11
Siemens Atellica IM Humidity Pack Recall Due to Software Error
Siemens Healthcare Diagnostics is recalling Atellica IM Humidity Packs because a software error causes the analyzer to incorrectly eject them as expired.
Product
Atellica IM Humidity Pack (Qty 5), SMN 11313505, UDI 00630414234526, Software Version V1.21.0 and lower - Product Usage: The system is intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric, chemiluminescent, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0795-2020·2020-03-11
Sticky Fingers Bakeries Gluten-Free Scones Recalled for Wheat Ingredient
Custom Foods LLC is recalling Sticky Fingers Bakeries Gluten-Free Scones because wheat is listed in the ingredients, posing a risk to individuals with celiac disease or gluten sensitivity.
Product
Sticky Fingers Bakeries Gluten-Free Scones, Quick & Easy Mix, Meyer Lemon; Net Wt. 14 oz. (0.875 LBS) 396.9g. In Ingredient list: Lemon Flavored Pieces {sugar, enriched wheat flour (wheat flour, niacin, reduced iron Thiamin mononitrate, riboflavin, folic acid) Sticky…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1436-2020·2020-03-11
Siemens Atellica IM Humidity Pack Software Error Recall
Siemens Healthcare Diagnostics is recalling Atellica IM Humidity Packs due to a software error that causes the analyzer to incorrectly eject them as expired.
Product
Atellica IM Humidity Pack (Qty 1), SMN 11313496, UDI 00630414243726, Software Version V1.21.0 and lower - Product Usage: Product Usage: The system is intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0862-2020·2020-03-11
Teva Recalls Mesalamine Tablets Due to Dissolution Test Failures
Teva Pharmaceuticals USA is recalling 3,695 bottles of Mesalamine Delayed-Release Tablets because stability testing showed low dissolution results.
Product
MESALAMINE — MESALAMINE (MESALAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1408-2020·2020-03-11
Medtronic Recalls McGRATH X3 Disposable Laryngoscope Blades Due to Fit Issues
Medtronic is recalling McGRATH X3 Disposable Laryngoscope Blades because they may not fit the video laryngoscope handle or fit too tightly, potentially affecting optical performance.
Product
McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video Laryngoscope to aid the intubation of the trachea Code: X3-002-000 (Individual Unit); X3-003-000 (Carton of 10 Units) - Product Usage: is a tool used to aid the intubation of the trachea. As a rigid…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1438-2020·2020-03-11
Polymer Technology Systems Recalls PTS Detect Cotinine In Vitro Diagnostic
Polymer Technology Systems is recalling PTS Detect Cotinine in vitro diagnostic devices due to a lack of FDA 510(k) clearance.
Product
PTS Detect Cotinine, Ref. No. 3061, UPC 381933061017 in vitro diagnostic - Product Usage: The PTS Detect cotinine system provides quantitative measurement of the nicotine metabolite cotinine (25 200 ng/mL) in capillary (fingerstick) or venous whole blood. The test is for…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1441-2020·2020-03-11
Advanced Bionics Recalls SoundWave Professional Suite Software 3.2
Advanced Bionics is recalling SoundWave Professional Suite Software 3.2 because the installation process fails when using the supplied USB drive, though current software versions remain functional.
Product
SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical SoundWave Professional Suite 3.2, CE 0123 - Product Usage: Soundwave 3.2 is used by healthcare professionals to program Advanced Bionics sound processors for use with…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0964-2020·2020-03-11
Axia Pharmaceutical Recalls Magnesium Chloride Injection Due to Sterility Concerns
Axia Pharmaceutical is recalling specific lots of Magnesium Chloride Injection because the company cannot assure the product's sterility.
Product
Magnesium Chloride Injection, MAGNESIUM CHLORIDE 20% INJECTABLE, For IV Use, 50 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0225-5
Category
Drug
Distribution
Distributed nationwide