The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53826–53850 of 73850

  • HighFDA (Devices)·Z-1565-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

    Stryker Instruments is voluntarily recalling CBCII Wound Drains and Ambulating Bulbs due to a potential sterility breach in the packaging.

    Product
    1/8 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1594-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    98" (249 cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Trifuse Ext Set w/2 MicroClave, Rotating Luer, Non-DEHP Tubing, Item No. B3338 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2157-2015·2015-05-13

    Spiceco Recalls Sylvia's Sizzlin' Hot Spice for Undeclared Peanut

    Spiceco is recalling Sylvia's Sizzlin' Hot Spice because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Sylvia's Sizzlin' Hot Spice, Net Wt. 5.5 oz. (156g), Distributed by: Sylvia Woods Food Company, P.O. Box 240, Harlem, NY 10027, UPC 608623000515
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2159-2015·2015-05-13

    Spiceco Recalls Fiesta Seasoned Salt for Undeclared Peanut

    Spiceco is recalling Fiesta Seasoned Salt because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Fiesta Seasoned Salt Net Wt 16 oz (1 LB) 454 g Distributed By Fiesta Mart Houston TX 77246-7481
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1591-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling specific MicroClave T-Connectors because they may separate, causing fluid leakage.

    Product
    113" (287cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Smallbore Quadfuse Ext Set w/MicroClave, 4 Clamps (Blue, 2 Red, White), Rotating Luer, Non-DEHP Tubing, Item No. B33303 Product Usage: IV Administration sets are intended for the infusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1590-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation

    ICU Medical is recalling 1,500 MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    104" (264 cm) Transfer Set w/MicroClave T-Connector, Check Valve, Smallbore Trifuse Ext w/2 MicroClave, Anti-Siphon Valve, 3 Clamps (White, Red, Blue), Rotating Luer, Non-DHEP Tubing, Item No. B33065 Product Usage: IV Administration sets are intended for the infusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2164-2015·2015-05-13

    Spiceco Recalls Sweet Hungarian Paprika for Undeclared Peanut

    Spiceco, Inc. is recalling Pride of Szeged Sweet Hungarian Paprika and other products because they may contain undeclared peanut protein.

    Product
    Maison Royal labeled as ordered
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1592-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling 13,800 MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    108" (274 cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V282000·2015-05-13

    Dodge Challenger Recall for Loose Side Air Bag Mounting Bolt

    Chrysler is recalling 2015 Dodge Challengers because a loose or missing rear mounting bolt on the driver's side air bag curtain may increase injury risk in a crash.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2168-2015·2015-05-13

    Spiceco Recalls Chicken Seasoning and Paprika for Undeclared Peanut

    Spiceco is recalling Better Valu Chicken Seasoning and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.

    Product
    Better Valu Chicken Seasoning Net. Wt. 5.25 oz (149 g) Distributed by: Federated Group, Inc. 3025 W. Salt Creek Lane Arlington Heights, IL 6005 www.better-valu.com UPC 079807003794
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1563-2015·2015-05-13

    Stryker Recalls Wound Drains Due to Potential Sterility Breach

    Stryker Instruments is voluntarily recalling specific wound drain products because the packaging may have a sterility breach.

    Product
    3/16 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1571-2015·2015-05-13

    Stryker Recalls Curved Trocar Wound Drains for Potential Sterility Breach

    Stryker Instruments is voluntarily recalling 1/8 in. Curved Trocar with Wound Drain devices due to a potential sterility breach in the packaging.

    Product
    1/8 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0992-2015·2015-05-13

    Cody Laboratories Recalls C-Topical 4% Cocaine Hydrochloride Due to Labeling Error

    Cody Laboratories is recalling 19,139 bottles of C-Topical 4% cocaine hydrochloride because they were incorrectly labeled as 10 mL instead of 4 mL.

    Product
    C-Topical 4% CII (cocaine hydrochloride), topical solution, 4 ml bottle, (NDC 0527-1728-74), Rx Only, Manufactured for Lannett Company, Inc. Philadelphia, PA 19136 by Cody Laboratories, Inc. Cody, WY 82414
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0975-2015·2015-05-13

    Wockhardt Recalls Captopril Tablets for Thickness Specification Failures

    Wockhardt USA is recalling specific lots of Captopril Tablets 12.5 mg because they failed to meet thickness specifications.

    Product
    Captopril Tablets, USP 12.5 mg, Rx Only, a) 100 count bottles NDC 64679-902-01, b) 1000 count bottles NDC 64679-902-02, Manufactured by Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt USA LLC., 20 Waterview Boulevard, Parsippany, NJ 07054 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1572-2015·2015-05-13

    Stryker Recalls Curved Trocar Wound Drains for Sterility Breach

    Stryker Instruments is voluntarily recalling 1/4 in. Curved Trocar with Wound Drain devices due to a potential sterility breach in the packaging.

    Product
    1/4 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1566-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

    Stryker Instruments is voluntarily recalling CBCII Wound Drains and Ambulating Bulbs due to a potential sterility breach in the packaging.

    Product
    1/4 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2015·2015-05-13

    Stryker Recalls Curved Trocar Wound Drains for Sterility Breach

    Stryker is voluntarily recalling 3/16 in. Curved Trocar with Wound Drain devices due to a potential sterility breach in the packaging.

    Product
    3/16 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1581-2015·2015-05-13

    Siemens ACUSON SC2000 Ultrasound Systems Recalled for Image Capture Failures

    Siemens is recalling 186 ACUSON SC2000 ultrasound systems because they may fail to capture images or clips during routine scans.

    Product
    ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C, VA16D and VA16E. Model 10433816. Product Usage: The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0983-2015·2015-05-13

    Romark Recalls Alinia Powder for Oral Suspension Due to Stability Failure

    Romark Laboratories is recalling specific lots of Alinia (nitazoxanide) powder for oral suspension because the product failed to meet long-term stability specifications for viscosity.

    Product
    Alinia (nitazoxanide), powder for oral suspension, 100mg/5mL, 60 mL/bottle. Rx only, Manufactured for Lupin Pharmaceuticals Inc, Baltimore, Maryland 21202 for Romark Laboratories 3000 Bayport Dr. Suite 200, Tampa, FL 33607
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1587-2015·2015-05-13

    Stryker Universal Battery Charger Recalled for Software Data Transmission Issue

    Stryker is recalling 223 Universal Battery Chargers because they are not transmitting usage data to the Stryker Cloud as designed. A software correction is being initiated.

    Product
    Universal Charger Product Usage: The Stryker Universal Battery Charger is designed to be used in conjunction with and provide power to non-sterile and sterile batteries. The Stryker Universal Battery Charger is a four station, modular battery charger intended to charge…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E038000·2015-05-12

    Fleetline Recalls Fender Brackets Due to Insufficient Welds

    Fleetline is recalling specific Nu-Line and Fleetline fender brackets and kits due to insufficient welds that may cause fender separation.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15133·2015-05-12

    IKEA Recalls Pressure-Mounted Safety Gates Due to Fall Hazard

    IKEA is recalling PATRULL KLÄMMA and PATRULL SMIDIG safety gates because they may fail to hold in place, posing a fall hazard. Consumers should stop using the gates and return them for a refund.

    Product
    PATRULL KLÄMMA and PATRULL SMIDIG Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V279000·2015-05-12

    Ford Recalls 2015 F-150 Trucks for Steering Shaft Rivet Defect

    Ford is recalling 2015 F-150 trucks because an improperly riveted steering shaft could separate, causing loss of steering control and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V278000·2015-05-12

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Brake Caliper Leaks

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon trucks because front brake calipers may leak fluid, increasing stopping distance and crash risk.

    Product
    GMC — GMC, CHEVROLET CANYON, COLORADO
    Category
    Vehicle
    Distribution
    Distributed nationwide