The Recall Desk

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.

50976–51000 of 73840

  • SevereFDA (Drugs)·D-0255-2016·2015-11-25

    US Compounding Recalls Hyaluronic Acid Syringes Due to Sterility Concerns

    US Compounding Inc is recalling 5,118 syringes of Hyaluronic Acid/Lidocaine PF due to deficient practices that may impact sterility assurance.

    Product
    Hyaluronic Acid/Lidocaine PF (20 mg/1%), 2 mL Single-Use Syringe , For Intra-Articular Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3087-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0372-2016·2015-11-25

    Downing Labs Recalls Piracetam Injection Due to Sterility Assurance Concerns

    Downing Labs, LLC is recalling Piracetam Injection, 200mg/mL, 10mL vials due to a lack of assurance of sterility. The recall covers all lots distributed nationwide and internationally.

    Product
    Piracetam Injection, 200mg/mL,10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-332-2016·2015-11-25

    Essential Wellness Pharma Recalls TRIMIX #1 Injection Due to Sterility Concerns

    Essential Wellness Pharma is recalling TRIMIX #1 Injection vials because poor production practices may have compromised the sterility of the compounded sterile preparations.

    Product
    TRIMIX #1 Injection, 4.2 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0285-2016·2015-11-25

    Prism Medical P-300 Portable Consumer Lift Recalled for Drive Shaft Failure

    ErgoSafe Products is recalling 1,721 Prism Medical P-300 Portable Consumer Lifts because the drive shaft and over speed arm may fail, potentially causing a patient to fall.

    Product
    Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300 lbs. /136 kg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0292-2016·2015-11-25

    US Compounding Recalls Vitamin D3 Vials Due to Sterility Concerns

    US Compounding Inc is recalling 55 vials of Vitamin D3 in Olive Oil due to deficient practices that may impact sterility assurance.

    Product
    Vitamin D3 in Olive Oil (50,000 IU/mL) 30 mL vial, For IM Use only, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3277-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0296-2016·2015-11-25

    Fresenius Modified Mixer Motor Recalled Due to Fire Risk

    Fresenius Medical Care is recalling 992 Modified Mixer Motors for 132 Gallon Dissolution Units because they lack full thermal protection, posing a fire hazard.

    Product
    Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units), P/N 160075. For Use in the Preparation of acid concentrate for hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0256-2016·2015-11-25

    US Compounding Recalls Hyaluronic Acid Syringes Due to Sterility Concerns

    US Compounding Inc is recalling 531 hyaluronic acid and lidocaine syringes because deficient practices may have impacted sterility assurance.

    Product
    Hyaluronic Acid/Lidocaine PF (60 mg/2%), 3 mL Single Use Syringe, For Intra-Articular Injection , Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3249-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0209-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part Case"***Sysco Imperial ***FIESTA VEGETABLE BLEND***REORDER# ***8446007 *** 6/4 lb*** (UPC) 1 00 74865 52887 7***INGREDIENTS: Broccoli, Carrots, White…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0310-2016·2015-11-25

    Ameditech Recalls Benzodiazepine Drug Abuse Tests Due to Reduced Reactivity

    Ameditech is recalling EDI BZO Uncut Sheet-Card drug abuse tests because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.

    Product
    EDI BZO UNCUT SHEET-CARD, Item No. 100170 These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0203-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling 32-ounce bags of First Street Italian Vegetable Blend due to potential Listeria monocytogenes contamination.

    Product
    Italian Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***FIRST STREET***ITALIAN BLEND CARROTS, CAULIFLOWER, ITALIAN GREEN BEANS, ZUCCHINI, LIMA BEANS*** NET WT 32 OZ***" UPC on bag 041512081958; Shipping Case UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0287-2016·2015-11-25

    Civco Needle Guide Starter Kit Recalled Due to Sterility Concerns

    Civco Medical Instruments is recalling 508 boxes of Needle Guide Starter Kits because the sterility of the product cannot be assured.

    Product
    CIVCO Needle Guide Starter Kit, Reusable non-sterile bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REFs 674-030, 674-030-T, 674-031, 674-031-T, 674-035, 674-036, 674-044, 674-052, 674-059, 674-061. Large Gauge Infiniti Plus Needle Guides, used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0306-2016·2015-11-25

    Ameditech Recalls DrugCheck Waived 12 Panel Cup Tests

    Ameditech is recalling DrugCheck Waived 12 Panel Cup tests because they have shown reduced reactivity.

    Product
    DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5 These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0201-2016·2015-11-25

    National Frozen Foods Recalls Italian Green Beans for Listeria Risk

    National Frozen Foods Corporation is recalling frozen Italian green beans due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Italian Green Beans. Product is IQF frozen, not ready to eat, each label carries cooking instructions. Packages sizes: 14 oz.; 16 oz.; 2 lbs.; 2.5 lbs.; 20 lbs. and 1,350 lbs. (tote) Product is sold under brands: Birds Eye (C&W), Markson First Crop, Bountiful Harvest…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0204-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***SIMPLOT CLASSIC*** ITALIAN BLEND*** INGREDIENTS: ZUCCHINI, CARROTS, CAULIFLOWER, ITALIAN BEANS, LIMA BEANS, RED BELL PEPPER***" For 12/2 lb UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0205-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling Sysco Classic and Imperial Italian Vegetable Blend due to potential Listeria monocytogenes contamination.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***Sysco Classic Italian Vegetable Blend***NET WT***2 LB***INGREDIENTS: Zucchini, Carrots, Cauliflower, Italian Green Beans, Baby Lima Beans***UPC 0…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0365-2016·2015-11-25

    Downing Labs Recalls Hydroxocobalamin Injection Due to Sterility Concerns

    Downing Labs, LLC is recalling 106 vials of Hydroxocobalamin Injection due to a lack of assurance of sterility. The product was distributed nationwide and internationally.

    Product
    Hydroxocobalamin Injection (Buffered) 1mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0301-2016·2015-11-25

    Ameditech Recalls 11 Panel Dip Cards Due to Reduced Reactivity

    Ameditech is recalling 11 Panel Dip Cards (OPI 2000 and OPI 300) because they have shown reduced reactivity. The recall covers 150 units distributed in the US and Australia.

    Product
    11 Panel Dip Card (OPI 2000), Item No. 11125AA2K; 11 Panel Dip Card (OPI 300) w/Adult, Item No. 11125AA These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0289-2016·2015-11-25

    Civco PercuNav Tracking Bracket Recalled Due to Sterility Concerns

    Civco Medical Instruments is recalling PercuNav tracking bracket kits because the sterility of the product cannot be assured.

    Product
    CIVCO Tracking Bracket Starter Kit, Reusable non-sterile PercuNav tracking bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REF 667-132. Large Gauge Infiniti Plus Needle Guides, used in needle-guided (or catheter) procedures with diagnostic ultrasound…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0313-2016·2015-11-25

    Ameditech Recalls Micro Screen 6 Panel Drug Abuse Test Cups

    Ameditech is recalling Micro Screen 6 Panel Cup drug abuse tests because they have shown reduced reactivity.

    Product
    Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0273-2016·2015-11-25

    Philips ECG Sync Cables Recalled for Electrical Interference Risk

    Philips is recalling ECG sync cables used with HeartStart monitors because electrical interference can cause misinterpretation of heart signals or interrupt pacing.

    Product
    ECG Out Cable,for use with a Philips ALS monitor/ defibrillator and bedside monitor for Synchronized cardioversion and Transcutaneous pacing. M1783A/M5526A 12-pin Sync cables, used with HeartStart MRx and HeartStart XL and HeartStart XL+
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0202-2016·2015-11-25

    National Frozen Foods Recalls Italian Blend for Listeria Risk

    National Frozen Foods is recalling Target-exclusive Italian Blend frozen vegetables due to potential Listeria monocytogenes contamination.

    Product
    Italian Blend. Product is IQF frozen, not ready to eat, each label carries cooking instruction. Label reads in part: "*** market pantry *** STEAM-IN-BAG Italian-Style Blend Broccoli, Cauliflower, Carrots, Italian-Style Green Beans & Zucchini*** NET WT 12 OZ***(UPC) 0 85239…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0207-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***MARKON FIRST CROP*** A proof of the label was provided, it does not contain product identity, net wt or ingredients. This product is available in…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V798000·2015-11-25

    Forest River Recalls Motorhomes Due to Unstable Electric Entry Steps

    Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, GEORGIE BOY PATHFINDER, PURSUIT, RIDGEVIEW, MIRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide