State

Northern Mariana Islands product recalls

72,971 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 22
Critical: 0
Severe: 8
Most recent: 2025-02-05

Of the 22 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 8 (36%) are Severe.

Which agencies issued them

These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5626–5650 of 72993

HighFDA (Food)·H-0384-2025·2025-08-13
Queen Bee Gardens whipped honey may contain stainless steel flakes
Queen Bee Gardens Whipped Honey Huckleberry in 11 oz jars is being recalled because the product may have small flakes of stainless steel in it. 24 jars are affected.
Product
Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182259. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0574-2025·2025-08-13
Spironolactone 25 mg tablets recalled after aluminum was found in product
Spironolactone Tablets USP 25 mg are being recalled because of the presence of a foreign substance identified as aluminum. 11,328 bottles are affected.
Product
SPIRONOLACTONE — SPIRONOLACTONE (SPIRONOLACTONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2272-2025·2025-08-13
epoc BUN test cards may show a negative sodium bias
epoc BGEM BUN Test Cards are being recalled because a negative sodium bias may exist in some lots, with an observed average bias of -4.4 mmol/L. 37,554 units are affected.
Product
epoc BGEM BUN Test Card [25pk]. Material Number: 10736515.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0383-2025·2025-08-13
Queen Bee Gardens pure whipped honey may contain stainless steel flakes
Queen Bee Gardens Whipped Honey Pure in 11 oz jars is being recalled because the product may have small flakes of stainless steel in it. 112 jars are affected.
Product
Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182006. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0568-2025·2025-08-13
Direct Rx duloxetine 30 mg capsules exceed the interim nitrosamine limit
Duloxetine Delayed-Release 30 mg capsules packaged by Direct Rx are being recalled because a nitrosamine drug substance related impurity was present above the proposed interim limit. 875 bottles affected.
Product
Duloxetine D/R, 30 mg, 30 Caps, RX Only, Packaged as a) 30-count bottle NDC 61919-0482-30, b) 60-count bottle, NDC 61919-0482-60, c) 90-count bottle, NDC 61919-0482-90; Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0552-2025·2025-08-13
Duloxetine 60 mg capsules exceed the safety assessment limit for nitrosamine
Duloxetine Delayed-Release Capsules USP 60 mg distributed by Breckenridge are being recalled because N-nitroso-duloxetine was present above the safety assessment limit. 1,829 bottles affected.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0382-2025·2025-08-13
Queen Bee Gardens raspberry whipped honey may contain stainless steel flakes
Queen Bee Gardens Whipped Honey Raspberry in 11 oz jars is being recalled because the product may have small flakes of stainless steel in it. 129 jars are affected.
Product
Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182358. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2277-2025·2025-08-13
Stryker SmartPump tourniquet cuff flanges may detach from the bladder
Stryker SmartPump Tourniquet disposable cuffs are being recalled because the cuff flange may become detached from the bladder, which the manufacturer links to a risk of hemorrhage if a leak occurs during a procedure.
Product
Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK / 5921-018-235; DISP 24X4,1BLA, 2PRT QUICK / 5921-024-235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0566-2025·2025-08-13
Doxepin hydrochloride capsules exceed the interim nitrosamine impurity limit
Doxepin Hydrochloride Capsules USP 10 mg from Alembic are being recalled because a nitrosamine drug substance related impurity was present above the proposed interim limit. 9,492 bottles affected.
Product
DOXEPIN HYDROCHLORIDE — DOXEPIN HYDROCHLORIDE (DOXEPIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2269-2025·2025-08-13
UniCel DxI 600 analyzer motor current resets below the required setting
UniCel DxI 600 Access Immunoassay Analyzers are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 271 systems are affected.
Product
UniCel DxI 600 Access Immunoassay Analyzer, Part Number A30260
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2238-2025·2025-08-13
BD Trucount control kits carry incorrect standard deviation values for beads
BD Trucount Controls 30 Test kits are being recalled because they contain incorrect standard deviation values for the low and high control beads, which compromises accurate bead count calculation. 629 kits affected.
Product
BD Trucount Controls, 30 Test - REF: 340335
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0572-2025·2025-08-13
Xolair 75 mg syringes exposed to temperatures outside labeled storage requirements
Xolair (omalizumab injection) 75 mg/0.5 mL is being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 4 units affected.
Product
XOLAIR — XOLAIR (OMALIZUMAB)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2271-2025·2025-08-13
DxI 600 with Spot B analyzer motor current resets below requirement
DxI 600 Access Immunoassay Analyzers with Spot B are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 177 systems are affected.
Product
DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2265-2025·2025-08-13
T4 Total ELISA kit box expiry exceeds the standards' shelf life
T4 Total ELISA kits are being recalled because the expiration date on the kit box label and Certificate of Analysis exceeded the shelf life of the standards and control solutions by two months. 47 units affected.
Product
Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Model/Catalog Number: EIA-4568 Product Description: T4 Total ELISA
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0573-2025·2025-08-13
Recombinate antihemophilic factor vials exposed to temperatures outside labeled storage
Recombinate [Antihemophilic Factor (Recombinant)] 5 mL vials are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 3 units affected.
Product
RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2270-2025·2025-08-13
DxI 600 immunoassay analyzer motor current resets below the required setting
A DxI 600 Access Immunoassay Analyzer is being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results.
Product
DxI 600 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71461
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2237-2025·2025-08-13
BD Trucount 664343 control kits carry incorrect standard deviation values
BD Trucount Controls 30 Test kits, REF 664343, are being recalled because they contain incorrect standard deviation values for the low and high control beads. 10 kits are affected.
Product
BD Trucount Controls, 30 Test - REF: 664343, RxOnly, IVD
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2266-2025·2025-08-13
UniCel DxI 800 analyzer motor current resets below the required setting
UniCel DxI 800 Access Immunoassay Analyzers are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results. 2,203 systems affected.
Product
UniCel DxI 800 Access Immunoassay Analyzer, Part Number 973100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0571-2025·2025-08-13
Xolair auto-injectors exposed to temperatures outside labeled storage requirements
Xolair (omalizumab injection) 150 mg/mL auto-injectors are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 6 units affected.
Product
XOLAIR — XOLAIR (OMALIZUMAB)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2268-2025·2025-08-13
DxI 800 with Spot B analyzer motor current resets below requirement
DxI 800 Access Immunoassay Analyzers with Spot B are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 451 systems are affected.
Product
DxI 800 Access Immunoassay Analyzer W/Spot B, Part Number A71456
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2267-2025·2025-08-13
DxI 800 immunoassay analyzer motor current resets below the required setting
A DxI 800 Access Immunoassay Analyzer is being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results.
Product
DxI 800 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71457
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V522000·2025-08-12
IC Bus school bus parking brake springs may corrode and break
International is recalling certain 2024-2026 IC Bus CESB and 2025 EVSB school buses because the parking brake tension spring may corrode and break, disengaging the parking brake. 3,230 buses affected.
Product
IC BUS — IC BUS CESB, EVSB
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V525000·2025-08-12
Heil Recalls 2018-2020 Front End Loader Garbage Trucks Due to Fire Risk
The Heil Co. is recalling 2018-2020 front end loader garbage trucks because excessive vibrations may cause hydraulic tubes to leak, increasing the risk of fire.
Product
HEIL — HEIL FRONT END LOADER GARBAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V524000·2025-08-12
Heil Recalls 2021-2022 Front End Loader Garbage Trucks Due to Weld Defect
The Heil Co. is recalling 2021-2022 front end loader garbage trucks because missing vertical welds on the automatic front loader arm may cause it to crack and fall, increasing injury risk.
Product
HEIL — HEIL FRONT END LOADER GARBAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V523000·2025-08-12
Heil Recalls 2024 Front End Loader Garbage Trucks for Fuel Solenoid Defect
The Heil Co. is recalling 2024 front end loader garbage trucks because a fuel shutoff solenoid may fail, causing the engine to stall while driving and increasing crash risk.
Product
HEIL — HEIL FRONT END LOADER GARBAGE
Category
Vehicle
Distribution
Distributed nationwide