The Recall Desk

State

Northern Mariana Islands product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19276–19300 of 73399

  • ModerateFDA (Drugs)·D-1415-2022·2022-08-31

    Alka Seltzer Extra Strength 24 CT Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Alka Seltzer Extra Strength 24 CT due to products stored outside proper temperature conditions, which may affect product quality.

    Product
    ALKA SELTZER EXTRA STRENGTH 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1435-2022·2022-08-31

    Four Topical Analgesic Products Recalled for Improper Storage Conditions

    Four topical analgesic products distributed to Family Dollar stores were recalled due to CGMP violations involving improper storage temperature conditions. No illnesses or injuries have been reported.

    Product
    ARTHRITIS HOT CREME 3 OZ SKU 901452 ICY HOT PATCH 1 CT SKU 911030 ICY HOT MUSCLE RUB 1.25 OZ SKU 920205 ICY HOT NO MESS 1.5 OZ SKU 998751 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1417-2022·2022-08-31

    Omeprazole Tablets Recalled Due to Improper Storage Conditions

    Good Sense and Prilosec OTC omeprazole tablets distributed by Family Dollar Stores have been recalled due to improper storage temperature conditions. No illnesses have been reported.

    Product
    GOOD SENSE OMEPRAZOLE TABLET 14CT SKU 900055 PRILOSEC OTC TABLET 14 CT SKU914128 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1636-2022·2022-08-31

    Fisher Scientific Swabs Recalled for Temperature Excursion During Storage

    Mckesson Medical-Surgical Inc. is recalling Fisherbrand laboratory swabs due to facility temperature excursions from June through August 2021 that may have impacted product effectiveness. All affected lots distributed between June 1 and September 30, 2021 are included.

    Product
    FISHER SCIENTIFIC Fisherbrand SWAB, ROUND BOTTOM CLR (50/PK)FSHSCI Catalog # 1490712
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1396-2022·2022-08-31

    Preferred Urinary Pain Relief Product Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Preferred Urinary Pain Relief Max Strength due to CGMP violations involving improper storage temperature. Product was distributed nationwide April 30 through June 10, 2022.

    Product
    PREFERRED URINRY PN RLF MAX STRNGTH 12 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1421-2022·2022-08-31

    RIC Stool Softener Recalled Due to Storage Temperature Deviations

    RIC Stool Softener Softgels (SKUs 917000 and 902493) distributed to Family Dollar Stores nationwide from April 30, 2022 through June 10, 2022 are recalled due to improper storage temperature conditions.

    Product
    RIC STOOL SOFTENER SOFTGEL 100 CT SKU 917000 RIC STOOL SOFTNER 100 CT SKU 902493 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1434-2022·2022-08-31

    Voltaren Arthritis Pain Gel Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Voltaren Arthritis Pain Gel 20G distributed April–June 2022 due to storage temperature deviations that may affect product effectiveness.

    Product
    VOLTAREN ARTHRITIS PAIN GEL 20G distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1618-2022·2022-08-31

    BD Vacutainer Blood Collection Tubes Recalled for Temperature-Exposure Effectiveness Loss

    BD Vacutainer blood collection tubes are recalled due to potential temperature damage during storage from June to August 2021. Affected tubes received between June 1 and September 30, 2021 may have reduced effectiveness.

    Product
    a. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 3.5ML PLAS VACUTAINER (100/BX), Model Number: 367983. b. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY8.5ML PLAS VACUTAINER (100/BX Model Number: 367988. c. BECTON DICKINSON BD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1440-2022·2022-08-31

    NPX Enema 4.5 FL OZ Two-Pack Recalled for Improper Storage

    Family Dollar Stores is recalling NPX Enema 4.5 FL OZ 2-packs due to improper storage conditions that violate manufacturing standards. The product was held outside appropriate temperature conditions at select Family Dollar stores between April 30 and June 10, 2022.

    Product
    NPX ENEMA 4.5 FL OZ 2 PK distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1637-2022·2022-08-31

    Total-Fix parasitology stool collection kit recalled for temperature exposure

    Mckesson is recalling a Total-Fix stool collection parasitology kit due to temperature exposure that may have reduced its effectiveness. All lots received between June 1 and September 30, 2021 are affected.

    Product
    MEDICAL CHEMICAL CORPORATION Total-Fix STOOL COLL KIT, TOTAL FIX PARASITOLOGY (100/CS) Catalog # NC0585129
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1375-2022·2022-08-31

    Antifungal spray and powder recalled for improper storage temperature conditions

    Family Dollar Stores recalled two antifungal products due to storage temperature deviations. The products may have been compromised in effectiveness due to failure to maintain proper storage conditions.

    Product
    DR SCHOLLS ANTI FUNGAL SPRAY PWDER 4.7 OZ SKU 998250 PREMIER ANTFGL TLNFTT LQ SPRY 5.3 FL OZ SKU 911077 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2022·2022-08-30

    Connoisseur’s Kitchen Recalls Imported Frozen Chicken Entrees Over Listeria Risk

    Connoisseur’s Kitchen is recalling approximately 880 pounds of imported frozen ready-to-eat chicken entrees due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Connoisseur’s Kitchen Recalls Imported Frozen Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E073000·2022-08-30

    Oshkosh Recalls Shepphard Steering Gears for S-Series 2.0 Vehicles

    Oshkosh is recalling certain Shepphard steering gears for S-Series 2.0 vehicles because incorrect assembly may cause the gear to fracture, potentially leading to a loss of steering control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V655000·2022-08-30

    Motorhomes with improperly routed hydraulic lines pose fire risk

    REV is recalling 2018-2023 motorhome models from Fleetwood and Holiday Rambler because hydraulic lines may be improperly routed or protected, risking fluid leaks that could cause fires. Dealers will repair free of charge.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VESTA, JAMBOREE, ADMIRAL, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V656000·2022-08-30

    Porsche Recalls Vehicles for Missing Headlight Adjustment Caps

    Porsche is recalling 2001-2020 models because missing caps on headlight adjustment screws can cause improper alignment, increasing crash risk.

    Product
    PORSCHE — PORSCHE CAYENNE TRANSSYBERIA, CAYENNE, PANAMERA, BOXSTER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V650000·2022-08-29

    Tiffin Wayfarer Motorhomes Recalled for Loose Wheel Lug Nuts

    Wayfarer is recalling 2017-2020 Tiffin Wayfarer motorhomes because wheel lug nuts may not have been properly tightened during a previous repair, posing a crash risk.

    Product
    TIFFIN — TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V652000·2022-08-29

    Audi Recalls 2022 A3, S3, and RS3 Models for Air Bag Defect

    Volkswagen Group of America is recalling 2022 Audi A3, S3, and RS3 vehicles because the front passenger air bag may be folded incorrectly, increasing injury risk in a crash.

    Product
    AUDI — AUDI A3, S3, RS 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V654000·2022-08-29

    Western Star 47X and 49X commercial trucks recalled for detaching hood bezel covers

    Daimler Trucks North America is recalling certain 2020-2023 Western Star 47X and 49X commercial trucks because hood bezel covers may detach, creating a road hazard and increasing crash risk. Approximately 3,498 vehicles are affected.

    Product
    WESTERN STAR — WESTERN STAR 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E072000·2022-08-29

    Cruise Recalls Automated Driving System Software for Left Turn Prediction Errors

    Cruise LLC is recalling Automated Driving System units with specific software versions that may incorrectly predict vehicle paths during unprotected left turns, increasing crash risk.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V653000·2022-08-29

    2022 Roadtrek Motorhomes Recalled for Loose Seat Mounting Bolts

    Roadtrek is recalling certain 2022 Zion, Zion SRT, Chase, and Zion Slumber motorhomes because front seat mounting bolts may be improperly tightened, potentially failing to restrain occupants during a crash.

    Product
    ROADTREK — ROADTREK ZION, ZION SRT, ZION SLUMBER, CHASE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V651000·2022-08-29

    2023 Kia Sportage: Loose Alternator Terminal Nut Poses Stall and Fire Risk

    Kia is recalling certain 2023 Sportage vehicles because the alternator battery positive terminal nut may loosen, risking engine stall or fire. Dealers will inspect and tighten the terminal nut free of charge.

    Product
    KIA — KIA SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V646000·2022-08-26

    Ford Recalls 2022 Mustang Mach-E for Rear Axle Shaft Defect

    Ford is recalling 2022 Mustang Mach-E vehicles because the right-rear axle half shafts may break under load, potentially causing loss of drive power or a rollaway.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide