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.

19826–19850 of 73399

  • HighFDA (Drugs)·D-1192-2022·2022-07-20

    Alpha Lipoic Acid injectable vials recalled for sterility assurance failure

    TMC Acquisition LLC is recalling Alpha Lipoic Acid 25mg/mL vials due to lack of assurance of sterility in manufacturing. The product was distributed nationwide.

    Product
    Alpha Lipoic Acid 25mg/mL, 30mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1194-2022·2022-07-20

    Compounded Testosterone-Anastrozole Injectable Vials Recalled for Sterility Concerns

    Tailor Made Compounding recalls 39 vials of a compounded injectable product for lack of assurance of sterility. Distribution was nationwide in the USA and Puerto Rico.

    Product
    Anastrozole/Testosterone Cypionate/Propionate 1mg/160mg/40mg/mL, 10 mL-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1234-2022·2022-07-20

    Testosterone injectable drug recall due to lack of sterility assurance

    TMC Acquisition LLC is recalling testosterone injectable products (58 vials) distributed nationwide and to Puerto Rico due to lack of assurance of sterility in manufacturing.

    Product
    Testosterone Cypionate/Enanthate 100/100mg/ml, a) 2 mL-vial, b) 4 mL-vial c) 10 mL-vial, Room temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1200-2022·2022-07-20

    Dexpanthenol Preservative Free Injectable Recalled Due to Sterility Assurance Failure

    Tailor Made Compounding recalls 84 vials of Dexpanthenol Preservative Free due to lack of assurance of sterility. The medication was distributed nationwide and in Puerto Rico.

    Product
    Dexpanthenol Preservative Free 250mg/mL, 2mL-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1361-2022·2022-07-20

    Medical device manufacturer recalls mislabeled interference screws nationwide

    SCIENCE & BIO MATERIALS has recalled ComposiTCP 30 Interference screws due to mislabeling. The recall affects 72 units distributed nationwide in the US.

    Product
    ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1375-2022·2022-07-20

    Cathcart Hip Ball prosthesis recalled for missing surgical technique specification

    DePuy Orthopaedics is recalling Modular Cathcart Hip Ball prostheses (sizes 41-60mm) because the Instructions for Use and Surgical Technique Guide did not document a +5mm offset specification. Updated guides now clarify this for hemi-hip arthroplasty procedures.

    Product
    MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000, 136342000, 136343000, 136344000, 136345000, 136346000, 136347000, 136348000, 136349000, 136350000, 136351000, 136352000, 136353000, 136354000…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1384-2022·2022-07-20

    Anti-FITC-AP CISH Kit Label Bears Incorrect Expiration Date

    Agilent Technologies is recalling 63 Anti-FITC-AP CISH Accessory Kits due to incorrect expiration dates on substrate vial labels, which may result in the use of expired materials.

    Product
    Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1418-2022·2022-07-20

    AloePro Aloe Vera Dietary Supplement Recalled Nationwide for Product Spoilage

    Premier Research Labs is recalling AloePro Aloe Vera dietary supplement nationwide due to product spoilage visible when opened. Consumers should discontinue use.

    Product
    AloePro Dietary Supplement Made With Organic ALOE VERA LIQUID 16 FL Oz. (475 mL) PREMIER RESEARCH LABS UPC Code: 80773500137 packaged in plastic HDPW bottles
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E060000·2022-07-19

    Cummins Recalls BP74E Battery Packs for Transit Bus Fire Risk

    Cummins is recalling BP74E battery packs used in transit buses because internal coolant leaks can cause short circuits and increase fire risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V510000·2022-07-19

    Thomas Built Buses Recalling School Buses Due to Seat Frame Cracking

    Daimler Trucks North America is recalling 2014-2023 Thomas Built Buses HDX and 2014-2022 EFX school buses because passenger seat frames may crack and rotate.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V509000·2022-07-19

    2022 Kia Sorento and Telluride recalled for spare tire brake defect

    Kia is recalling 2022 Sorento and Telluride vehicles with an incorrect spare tire that can impair the anti-lock braking and traction control systems. These defects increase the risk of a crash.

    Product
    KIA — KIA SORENTO, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E059000·2022-07-18

    Besser Pro Recalls Trailer Axles Due to Weld Defects

    Besser Pro is recalling 7000 lb Tubular Straight Axle assemblies for trailers because improper welds may cause cracking or separation, increasing crash risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V507000·2022-07-15

    Arcimoto hybrid electric vehicles high voltage connector latch defect

    Arcimoto is recalling certain 2019-2022 model year hybrid electric vehicles with a high voltage connector defect that may detach, causing sudden loss of power steering and drive power.

    Product
    ARCIMOTO — ARCIMOTO FUV, ROADSTER, DELIVERATOR, RAPID RESPONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2022·2022-07-15

    Ready Dough Pizza Recalls Pepperoni, Ham, and Bacon Products

    Ready Dough Pizza Inc. is recalling approximately 8,018 pounds of pizza products produced without federal inspection and containing undeclared allergens.

    Product
    Ready Dough Pizza Inc. Recalls Pepperoni Pizza Products Produced Without Benefit of Inspection and also Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E058000·2022-07-15

    Engineered Controls Recalls Propane Service Valves for Leak Risk

    Engineered Controls International is recalling specific propane service valves for recreational vehicles due to incorrect thread depth that may cause leaks.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V508000·2022-07-15

    Isuzu Recalls 2022 FTR and FVR Trucks Due to Engine Braking Defect

    Isuzu is recalling 2022 FTR and FVR trucks because a software error disables engine braking, potentially increasing stopping distances and crash risk.

    Product
    ISUZU — ISUZU FTR, FVR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V504000·2022-07-14

    2022 Chrysler and Dodge vehicles recalled for tire pressure monitoring sensor failure

    Chrysler and Dodge are recalling certain 2022 vehicles because TPMS sensors may fail prematurely, causing them to stop alerting drivers to low tire pressure. This can lead to tire failure and increase crash risk.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22758·2022-07-14

    Westfield Outdoor Recalls Outfitter and Big Horn Tents for Smoke Inhalation Hazard

    Westfield Outdoor is recalling approximately 5,050 Cabela's Outfitter and Big Horn camping tents because the stove jack ring can deteriorate under heat and create smoke inside the tent, posing a smoke inhalation risk.

    Product
    Outfitter and Big Horn tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22E057000·2022-07-14

    Chrysler Recalls Mopar Tire Pressure Sensors Due to Battery Failure

    Chrysler is recalling Mopar Tire Air Pressure Sensors because the battery may fail prematurely. This can cause the system to stop working, increasing the risk of a crash.

    Product
    TIRES:PRESSURE MONITORING AND REGULATING SYSTEMS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V505000·2022-07-14

    Blue Bird Recalls School Buses Due to Electrical Grounding Defect

    Blue Bird is recalling 2018-2022 school buses with Cummins electric drivetrains because an improperly grounded air compressor poses an electric shock risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22185·2022-07-14

    Sakar International Recalls Tony Hawk Silver Helmets Due to Head Injury Risk

    Sakar International is recalling about 12,655 Tony Hawk Silver Metallic multi-purpose helmets sold at Walmart from March to June 2022. The helmets do not meet federal safety standards for positional stability and retention, and may fail to protect in a crash.

    Product
    Tony Hawk Silver Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1402-2022·2022-07-13

    Prairie City Bakery Peanut Butter Chocolate Chip Cakes Recalled for Salmonella

    Prairie City Bakery is recalling Peanut Butter Chocolate Chip Ooey Gooey Butter Cakes due to Salmonella contamination from recalled Jif peanut butter ingredient. Products were distributed to gas stations and convenience stores nationwide.

    Product
    Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake 2oz. individual UPC: 7-9788436718-2; 10 individual units per display unit; 6 display units per wholesale case.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1319-2022·2022-07-13

    Palindrome HSI Chronic Catheter Recalled for Potential Hub Leaking

    Covidien is recalling Palindrome HSI Chronic Catheters due to a potential leaking condition in the catheter hub that may cause unanticipated fluid return during dialysis. Approximately 13,526 units distributed worldwide are affected.

    Product
    Palindrome HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1312-2022·2022-07-13

    Palindrome Precision Chronic Dialysis Catheter Hub Leak Risk

    Palindrome Precision Chronic Catheters used for dialysis may leak due to a flaw in the hub component, potentially allowing unintended fluid to escape during treatment.

    Product
    Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide