The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58351–58375 of 73856

  • HighFDA (Devices)·Z-1562-2014·2014-05-14

    AlloSource Recalls AlloFuse DBM Putty Due to Donor Hemodilution

    AlloSource, Inc. is recalling 29 units of AlloFuse DBM Putty 5cc because the donor was hemodiluted. The product is used as a bone graft extender in orthopedic applications.

    Product
    AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not intrinsic to the stability of the bony structure. AlloFuse is indicated to be packed gently into bony gaps in the skeletal system as a bone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1305-2014·2014-05-14

    Mangiacotti Ocean Hand Sanitizer Spray Recalled for Bacterial Contamination

    Mangiacotti is recalling Ocean Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria. Consumers should stop using the product.

    Product
    Mangiacotti - Ocean Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle, UPC 870678005320, Active Ingredient Benzalkonium Chloride 0.1%, Dist By: Mangiacotti, Attleboro, MA 02703.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1528-2014·2014-05-14

    INOmax DSIR Nitric Oxide Delivery System Recalled for Monitoring Anomaly

    INO Therapeutics is recalling 22 INOmax DSIR Nitric Oxide Delivery Systems due to a software anomaly that may trigger unintended alarms.

    Product
    INOmax DSIR, model 10007, Nitric Oxide Delivery System, with Software version 3.0.0. The INOmax DS delivery system delivers INOMAX (nitric oxide for inhalation) therapy gas and provides continuous monitoring of inspired O2, NO2, and NO, and a comprehensive alarm system. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1568-2014·2014-05-14

    Medtronic Refill Kits Recalled Due to Occluded Extension Tubing Sets

    Medtronic is recalling specific Refill Kits for implantable infusion pumps because some contain occluded extension tubing that prevents filling. No patient injuries beyond additional needle sticks have been reported.

    Product
    Refill Kit 8551/856X (includes Models 8561, 8562 and 8564) for use with Medtronic Implantable Programmable Infusion Pumps. Product Usage: The Refill Kits are intended for use in refilling Medtronic programmable, implantable infusion pumps with the exception of Medtronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14176·2014-05-14

    Cabela's Recalls Electronic Jerky Blaster Due to Fire Hazard

    Cabela's is recalling Electronic Jerky Blasters because the battery charger adapter can overcharge, causing the battery and adapter to overheat.

    Product
    Electronic Jerky Blaster
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1307-2014·2014-05-14

    Mangiacotti Pomegranate Hand Sanitizer Recalled for Bacterial Contamination

    Mangiacotti is recalling Pomegranate Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.

    Product
    Mangiacotti - Pomegranate Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle, UPC 870678005344, Active Ingredient Benzalkonium Chloride 0.1%, Dist By: Mangiacotti, Attleboro, MA 02703.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1563-2014·2014-05-14

    Mar Cor Purification Recalls Central Water Platform Reverse Osmosis Systems

    Mar Cor Purification is recalling 197 Central Water Platform (CWP) reverse osmosis systems because a specific lot of water inlet solenoid valves may fail, stopping water production.

    Product
    Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse osmosis system with the intended use of producing water for dialysis of multiple patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1554-2014·2014-05-14

    Bausch & Lomb Recalls Biotrue Multi-Purpose Contact Lens Solution

    Bausch & Lomb is recalling Biotrue Multi-Purpose Contact Lens Solution due to out-of-specification results for a disinfectant.

    Product
    Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1300-2014·2014-05-14

    Wockhardt Recalls Metoprolol Succinate Tablets for Dissolution Failure

    Wockhardt USA is recalling specific lots of Metoprolol Succinate Extended-Release Tablets because they failed dissolution testing at the nine-month time point.

    Product
    Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 30-count bottle, Rx only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054, USA; NDC 64679-735-09, UPC 3 64679 73509 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1569-2014·2014-05-14

    Shimadzu Digital Radiography X-Ray System Recalled for Image Loss

    Shimadzu Medical Systems is recalling its Digital Radiography X-Ray System because a report was received regarding lost images under certain circumstances.

    Product
    Shimadzu Digital Radiography X-Ray System, Catalog No. DAR-8000f. This device is intended to be used for radiography in the hospital with X-ray devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1304-2014·2014-05-14

    Mangiacotti Lavender Hand Sanitizer Recalled for Bacterial Contamination

    Mangiacotti is recalling Lavender Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria. Consumers should stop using the product.

    Product
    Mangiacotti - Lavender Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle, UPC 870678005313, Active Ingredient Benzalkonium Chloride 0.1%, Dist by: Mangiacotti, Attleboro, MA 02703 .
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1552-2014·2014-05-14

    Tenex TX1 Tissue Removal System Recalled for Packaging Defect

    Tenex Health Inc is recalling TX1 Tissue Removal Systems because cracks in the packaging may compromise the sterile barrier during transport in extreme cold.

    Product
    TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box), TX1 MicroTip P/N 554-1002-001 (inner tray). For use with the TX System Console as an ultrasonic surgical aspirator of soft tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1540-2014·2014-05-14

    Alere Triage BNP Test Recalled for Potential Out-of-Range Results

    Alere San Diego, Inc. is recalling specific lots of the Alere Triage BNP Test because they may not recover within range when tested with certain controls.

    Product
    Alere Triage BNP Test for the Beckman Coulter Access Family of Immunoassay Systems, Model Number 98200, Lot Numbers: 329599, 331265. The Alere Triage BNP test is intended to be used as an aid in the diagnosis of congestive heart failure (heart failure), as an aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1303-2014·2014-05-14

    Mangiacotti Lemon Verbena Hand Sanitizer Recalled for Bacterial Contamination

    Mangiacotti is recalling Lemon Verbena Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.

    Product
    Mangiacotti - Lemon Verbena Hand Sanitizer Spray, alcohol free, 0.5 fl. Oz., 15 mL spray bottle, UPC 870678005306, Active Ingredient Benzalkonium Chloride 0.1%, Dist by: Mangiacotti, Attleboro, MA 02703.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1313-2014·2014-05-14

    Boehringer Ingelheim Roxane Recalls Azathioprine Tablets Due to Incorrect Expiration Dates

    Boehringer Ingelheim Roxane Inc is recalling 8,304 bottles of Azathioprine Tablets USP, 50 mg, because they were labeled with 36-month expiration dates instead of the approved 24 months.

    Product
    Azathioprine Tablets USP, 50 mg, 100 count bottle, Rx only, Roxanne Laboratories, Inc., Columbus, Ohio, 43216, NDC 0054-4084-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1309-2014·2014-05-14

    Merck Recalls Liptruzet Tablets Due to Packaging Defects

    Merck & Co. is recalling Liptruzet tablets because packaging defects allowed air and moisture to enter, potentially affecting product effectiveness.

    Product
    Liptruzet (ezetimibe and atorvastin) tablets,10 mg/10 mg, a) 30 count blister (NDC 66582-320-30), b) 90 count blister (NDC 66582-320-54), Rx only, Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc, Whitehouse Station, NJ 08889
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1312-2014·2014-05-14

    Merck Recalls Liptruzet Tablets Due to Defective Outer Packaging

    Merck is recalling Liptruzet tablets because defective outer foil pouches may allow air and moisture to enter, potentially affecting product effectiveness.

    Product
    Liptruzet (ezetimibe and atorvastin) tablets,10 mg/80 mg, a) 30 count blister (NDC 66582-323-30), b) 90 count blister (NDC 66582-323-54), Rx only, Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc, Whitehouse Station, NJ 08889
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1311-2014·2014-05-14

    Merck Recalls Liptruzet Tablets Due to Packaging Defects

    Merck is recalling Liptruzet tablets because outer packaging defects allowed air and moisture to enter, potentially affecting product effectiveness.

    Product
    Liptruzet (ezetimibe and atorvastin) tablets,10 mg/40 mg, a) 30 count blister (NDC 66582-322-30), b) 90 count blister (NDC 66582-322-54), Rx only, Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc, Whitehouse Station, NJ 08889
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1310-2014·2014-05-14

    Merck Recalls Liptruzet Tablets Due to Packaging Defects

    Merck & Co. is recalling Liptruzet tablets because packaging defects allowed air and moisture to enter, potentially reducing product effectiveness.

    Product
    Liptruzet (ezetimibe and atorvastin) tablets,10 mg/20 mg, a) 30 count blister (NDC 66582-321-30), b) 90 count blister (NDC 66582-321-54), Rx only, Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc, Whitehouse Station, NJ 08889
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V244000·2014-05-13

    Supreme Corporation Recalls 2013 Transit Buses Due to Wheelchair Lift Fire Risk

    Supreme Corporation is recalling 116 model year 2013 transit buses and trolleys because an armored cable may not clear the wheelchair lift, posing a fire risk.

    Product
    STARTRANS — STARTRANS, SUPREME PRESIDENT, SENATOR II, ACTIVITY, SENATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V248000·2014-05-13

    Jerr-Dan Standard Duty Wreckers Recalled for Underlift Boom Drift

    Jerr-Dan is recalling 2007-2014 Standard Duty Wreckers because the underlift boom tilt cylinder may drift down during towing, increasing crash risk.

    Product
    JERR-DAN — JERR-DAN STANDARD DUTY WRECKER
    Category
    Vehicle
    Distribution
    Distributed nationwide