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.

51326–51350 of 73840

SevereFDA (Drugs)·D-0057-2016·2015-11-04
FDA Recalls Alprostadil/Procaine Injectable Solution Due to Sterility Concerns
The FDA is recalling 27 vials of Alprostadil/Procaine Injectable Solution because the manufacturer cannot ensure the product is sterile.
Product
ALPROSTADIL/PROCAINE, Injectable Solution, 40 MCG/0.1%/ML, 10 mL and 20 mL vials, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0063-2016·2015-11-04
FDA Recalls Chorionic Gonadotropin Syringes Due to Sterility Concerns
The FDA is recalling 834 syringes of Chorionic Gonadotropin compounded by Moses Lake Professional Pharmacy because the agency cannot ensure the product is sterile.
Product
CHORIONIC GONADOTROPIN, Injectable Solution,175 UNITS/1.5mg per syringe with Methylcobalamin, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0150-2016·2015-11-04
Moses Lake Pharmacy Recalls Six Trimix Syringes Due to Sterility Concerns
JD & SN Inc. is recalling six syringes of Trimix injectable solution because the company cannot guarantee the product's sterility.
Product
TRIMIX, injectable Solution, 30MG/1MG/20MCG, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0078-2016·2015-11-04
FDA Recalls Estradiol Pellets Due to Lack of Sterility Assurance
JD & SN Inc. is recalling Estradiol pellets because the FDA determined there is a lack of assurance of sterility for all sterile human compounded drugs within their expiry.
Product
ESTRADIOL, Pellet, 12.5 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0143-2016·2015-11-04
FDA Recalls Testosterone Cypionate Injection Due to Sterility Concerns
FDA is recalling Testosterone Cypionate for SubQ Injection from Moses Lake Professional Pharmacy due to lack of assurance of sterility.
Product
TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 200 mg/mL, syringe size: 5ml and 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·15V730000·2015-11-04
Blue Bird School Bus Wheelchair Lift Recall for Bearing Defects
Blue Bird is recalling certain school buses with Ricon wheelchair lifts where pivot holes may allow bearings to move, risking platform failure.
Product
BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, MICRO BIRD, CONVENTIONAL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0104-2016·2015-11-04
Kermit's Key Lime Barbecue Sauce Recalled for Undeclared Soy
Kermit, Inc. is recalling 16-ounce bottles of Key Lime Barbecue Sauce due to undeclared soy on the label.
Product
Kermit's Medium Mannered Key Lime Barbecue Sauce, 16 oz, Key West, FL, UPC 116601501409
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0161-2016·2015-11-04
Pfizer Recalls Subpotent Xanax Alprazolam Tablets Nationwide
Pfizer is voluntarily recalling 21,120 bottles of Xanax (alprazolam) 0.25 mg tablets because the medication contains less active ingredient than labeled.
Product
XANAX — XANAX (ALPRAZOLAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0102-2016·2015-11-04
Kermit's Key Lime Steak Sauce Recalled for Undeclared Soy
Kermit, Inc. is recalling 10-ounce bottles of Key Lime Steak Sauce because the label fails to list soy as an ingredient.
Product
Kermit's Key Lime Steak Sauce, 10 oz, Key West, FL, UPC 231920085093
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0118-2016·2015-11-04
Siemens CIOS ALPHA Fluoroscopic X-Ray System Recalled for Potential Failure
Siemens Medical Solutions is recalling 44 CIOS ALPHA fluoroscopic x-ray systems due to a potential system failure that could interrupt patient procedures.
Product
CIOS ALPHA; image intensified fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V731000·2015-11-04
Blue Bird Transit Buses Recalled for Wheelchair Lift Bearing Defect
Blue Bird is recalling 2007-2015 transit buses with Ricon wheelchair lifts where pivot holes may allow bearings to shift, risking platform failure.
Product
BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, MICRO BIRD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0177-2016·2015-11-04
Philips Recalls Brilliance Big Bore CT Systems Due to X-ray Measurement Error
Philips Medical Systems is recalling 268 Brilliance Big Bore CT systems worldwide due to X-ray measurement errors causing image artifacts.
Product
Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0160-2016·2015-11-04
LifeHealth Recalls BG Cartridges for IRMA TRUPOINT Blood Gas Analyzer
LifeHealth is recalling BG cartridges for the IRMA TRUPOINT Blood Gas Analyzer because the pH sensor may provide falsely elevated results as the product ages.
Product
BG cartridges for IRMA TRUPOINT Blood Gas Analyzer, PN 048103. BG Cartridge are single use, disposable, in vitro diagnostics intended for point of care (POC), professional, use with the IRMA TRUpoint¿ Blood Analysis System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0106-2016·2015-11-04
Kermit's Chipotle Key Lime Barbecue Sauce Recalled for Undeclared Soy
Kermit, Inc. is recalling 16 oz bottles of Chipotle Key Lime Barbecue Sauce due to undeclared soy on the label.
Product
Kermit's Chipotle Key Lime Barbecue Sauce, 16 oz, Key West, FL, UPC 091920850929
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0159-2016·2015-11-04
LifeHealth Recalls IRMA TRUPOINT Blood Gas Analyzer CC Cartridges
LifeHealth, LLC is recalling IRMA TRUPOINT Blood Gas Analyzer CC Cartridges because the pH sensor may provide falsely elevated results as shelf life progresses.
Product
CC cartridges for IRMA TRUPOINT Blood Gas Analyzer, PN 039903. The CC Cartridge are single use, disposable, in vitro diagnostics intended for point of care (POC), professional, use with the IRMA TRUpoint¿ Blood Analysis System.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V729000·2015-11-04
MobilityWorks Recalls Ford Vans with Defective Ricon Wheelchair Lifts
MobilityWorks is recalling 667 Ford E-series vans equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure the operator.
Product
FORD — FORD E-250, E-150, E-350
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0105-2016·2015-11-04
Kermit's Hot & Spicy Key Lime Barbecue Sauce Recalled for Undeclared Soy
Kermit, Inc. is recalling 16 oz bottles of Hot & Spicy Key Lime Barbecue Sauce due to undeclared soy on the label.
Product
Kermit's Hot & Spicy Key Lime Barbecue Sauce, 16 oz, Key West, FL, UPC 116601501423 & 802468905312
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0108-2016·2015-11-04
Kermit's Key Lime Ginger Wasabi Marinade Recalled for Undeclared Soy and Wheat
Kermit, Inc. is recalling 455 bottles of Key Lime Ginger Wasabi Marinade because the label fails to list soy and wheat ingredients.
Product
Kermit's Key Lime Ginger Wasabi Marinade, 12 oz, Key West, FL, UPC 070820060706 & 802468905480
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0139-2016·2015-11-04
Moses Lake Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns
JD & SN Inc. is recalling 13 vials of 80 mg testosterone pellets because the FDA cannot ensure the sterile compounded drugs are free from contamination.
Product
TESTOSTERONE, Pellet, 80 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0101-2016·2015-11-04
Kermit's Key Lime Cocktail Sauce Recalled for Undeclared Soy
Kermit, Inc. is recalling 12-ounce bottles of Key Lime Cocktail Sauce due to undeclared soy on the label.
Product
Kermit's Key Lime Cocktail Sauce, 12 oz, Key West, FL, UPC 007172006076 & 0802468905503
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0179-2016·2015-11-04
Encore Medical Recalls Turon Shoulder Impaction Fixtures Due to Material Wear
Encore Medical is recalling 277 Turon Shoulder Impaction Fixtures because polymer material wore off during assembly, potentially contaminating the implant.
Product
Turon Shoulder Impaction Fixture REF 804-15-102 The Turon and RSP Impaction Fixtures are used in the operating room on the back table to assemble the shoulder systems for implant. The Turon Fixture is used to connect the Humeral Head to the Humeral Neck, then subsequently to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0107-2016·2015-11-04
Kermit's P4 Hot Sauce Recalled for Undeclared Soy Allergen
Kermit, Inc. is recalling Kermit's P4 Hot Sauce because the product label fails to declare soy, a major food allergen.
Product
Kermit's P4 Hot Sauce, 5.5 oz, Key West, FL, UPC 020108012019 & 802468905701
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0103-2016·2015-11-04
Kermit's Key Lime Barbecue Sauce Recalled for Undeclared Soy
Kermit, Inc. is recalling 16 oz bottles of Key Lime Barbecue Sauce due to undeclared soy on the label.
Product
Kermit's Sweet & Tasty Key Lime Barbecue Sauce, 16 oz, Key West, FL, UPC 011550150134 & 802468905411
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0163-2016·2015-11-04
Abbott Recalls ARCHITECT i2000SR Systems Due to Incorrect Tubing
Abbott Laboratories is recalling 65 ARCHITECT i2000SR diagnostic systems worldwide because they contain incorrect tubing.
Product
ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The ARCHITECT system is designed to perform automated immunoassay tests, utilizing CMIA (chemiluminescent microparticle assay) detection technology.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0180-2016·2015-11-04
Encore Medical Recalls Reverse Shoulder Prosthesis Stem Impaction Fixtures
Encore Medical is recalling 634 units of Reverse Shoulder Prosthesis Stem Impaction Fixtures because polymer wear from the fixtures can damage the titanium coating on humeral stems during assembly.
Product
Reverse Shoulder Prosthesis Stem Impaction Fixture REF 804-03-053 The Turon and RSP Impaction Fixtures are used in the operating room on the back table to assemble the shoulder systems for implant. The Turon Fixture is used to connect the Humeral Head to the Humeral Neck, then…
Category
Medical Device
Distribution
Distributed nationwide