State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45251–45275 of 73832

ModerateFDA (Devices)·Z-0662-2017·2016-12-07
Spectranetics Recalls ELCA Coronary Atherectomy Catheters Due to Packaging Integrity
Spectranetics is voluntarily recalling ELCA Coronary Atherectomy Catheters and related devices because their outer sterile packaging may be compromised.
Product
ELCA Coronary Atherectomy Catheter. Models: 110-001, 110-002, 110-004, 114-009, 117-016, 117-205, 120-009 The Laser Catheters are used in conjunction with the Spectranetics CVX-300¿ Excimer Laser System and are intended for use in patients with single or multivessel coronary…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0156-2017·2016-12-07
Burel Pharmaceuticals Recalls UROLET MB Tablets Due to Manufacturing Deficiencies
Burel Pharmaceuticals is recalling UROLET MB Urinary Antiseptic tablets because manufacturing deficiencies may cause the product to fail potency or uniformity tests.
Product
UROLET MB URINARY ANTISEPTIC, ANTISPASMODIC Tablets, Each tablet contains: Methenamine 81.6 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue, 10.8 mg; Hyoscyamine Sulfate, 0.12 mg, (a) 30 count (NDC 35573-302-30) and (b) 100 count bottles (NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0689-2017·2016-12-07
MicroPort Recalls Cobalt Chromium Hip Replacement Heads Due to Metal Debris Risk
MicroPort Orthopedics is recalling specific Cobalt Chromium hip replacement heads because internal data showed an increasing trend in revision rates and a specific hazard of tissue reaction to metal debris.
Product
Cobalt Chromium Heads Transcend: 26000017, 26000018, 26000019, 26000020, 26000021, 26000022, 26000023, 26000024, 26000025, 26000026, 26000027, 26000028 Conserve: 38013800, 38013804, 38013835, 38014000, 38014004, 38014035, 38014200, 38014204, 38014235, 38014400…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0159-2017·2016-12-07
Burel Pharmaceuticals Recalls AZUPHEN MB Urinary Antiseptic Capsules
Burel Pharmaceuticals is recalling AZUPHEN MB Urinary Antiseptic Capsules due to manufacturing deviations that may cause assay or content uniformity failures.
Product
AZUPHEN MB URINARY ANTISEPTIC Capsules, Each capsule contains: Methenamine 120 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue 10 mg, Hyoscyamine Sulfate, 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0162-2017·2016-12-07
Burel Pharmaceuticals Recalls Phenazopyridine Hydrochloride Tablets Due to Manufacturing Deficiencies
Burel Pharmaceuticals is recalling specific lots of Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may result in assay or content uniformity failures.
Product
Phenazopyridine Hydrochloride Tablets, USP, 200 mg, 100 count bottles, Rx only, Manufactured for: Burel Pharmaceuticals, Inc., Richland, MS --- NDC 35573-306-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0166-2017·2016-12-07
Nationwide Laboratories Recalls Salsalate Tablets Due to Manufacturing Deviations
Nationwide Laboratories is recalling Salsalate Tablets, 750 mg, because they were manufactured under practices that may result in assay or content uniformity failures.
Product
Salsalate Tablets, USP, 750 mg, packaged in a) 100 count bottles (NDC 42937-704-10); b) 500 count bottles (NDC 42937-704-18); and c) 1000 count bottles (NDC 42937-704-20); Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0674-2017·2016-12-07
Terumo BCT Recalls Adiprep Adipose Transfer System Due to Labeling Error
Terumo BCT is voluntarily recalling 660 units of the Adiprep Adipose Transfer System because incorrect labeling could cause operator confusion.
Product
Adiprep Adipose Transfer System. Product Codes: 51431; 51432; 51433; 514001-347.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0667-2017·2016-12-07
Siemens Recalls Z6Ms Transesophageal Transducers Due to Material Deterioration
Siemens is recalling 33 Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems because the material covering the articulating section has deteriorated, causing acquisition errors.
Product
Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems, Z6Ms model 10436113. Radiology: The ACUSON SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transesophageal, Adult…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0682-2017·2016-12-07
Sorin Group Recalls Stöckert Heater Cooler System 3T for Disinfection Review
Sorin Group USA is recalling Stöckert Heater Cooler System 3T units to ensure strict adherence to disinfection and monitoring instructions.
Product
ST¿CKERT HeaterCooler System 3T; Item Number 160281, HeaterCooler 3T, 240V/60Hz; Item Number 160282, HeaterCooler 3T, 208V/60Hz; Item Number 160285, HeaterCooler 3T, 120V/ 60Hz The Heater Cooler 3T is used with a St¿ckert S3 heart lung machine and / or any other heart…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0663-2017·2016-12-07
Spectranetics Recalls Medical Devices Due to Compromised Sterile Packaging
Spectranetics is voluntarily recalling the Turbo Elite Atherectomy Catheter, ELCA Coronary Atherectomy Catheter, and Bridge Occlusion Balloon because their outer sterile packaging may be compromised.
Product
Bridge Occlusion Balloon. Model: 590-001 Temporary vessel occlusion of the superior vena cava in applications including perioperative occlusion and emergency control of hemorrhage. Any use for procedures other than those indicated in the instructions is not recommended.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0669-2017·2016-12-07
Terumo Recalls MISAGO RX Self Expanding Peripheral Stent
Terumo Medical Corp is recalling 7,965 MISAGO RX Self Expanding Peripheral Stents nationwide because they do not conform to product specifications regarding diameter and shape.
Product
MISAGO RX Self Expanding Peripheral Stem
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0167-2017·2016-12-07
Nationwide Laboratories Recalls Phenazopyridine Hydrochloride Tablets Due to Manufacturing Deviations
Nationwide Laboratories is recalling Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may result in assay or content uniformity failures.
Product
Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830, NDC 42937-701-10.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0165-2017·2016-12-07
Nationwide Laboratories Recalls Salsalate Tablets Due to Manufacturing Deviations
Nationwide Laboratories is recalling Salsalate Tablets, USP, 500 mg, because they were manufactured under practices that may result in assay or content uniformity failures.
Product
Salsalate Tablets, USP, 500 mg, packaged in a) 500 count bottles (NDC 42937-703-18); b) 100 count bottles (NDC 42937-703-10); and c) 1000 count bottles (NDC 42937-703-20); Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0672-2017·2016-12-07
Baxter Recalls SIGMA Spectrum Infusion Pump Rear Case Assemblies
Baxter Healthcare is recalling 439 V6 Rear Case Assemblies for SIGMA Spectrum Infusion Pumps because the speakers may fail prematurely.
Product
V6 Rear Case Assembly, Product Code 35701, a replacement part for the SIGMA Spectrum Infusion Pump -- SIGMA LLC Medina, NY 14103 --- NOTE: The speakers are a part of the rear case assembly located in the back of the infusion pump. The speaker is intended to generate audible…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0685-2017·2016-12-07
MicroPort Orthopedics Recalls Procotyl Rim-Lock Liners Due to Tissue Reaction Risk
MicroPort Orthopedics is recalling 500 units of Procotyl Rim-Lock Liners because revision rate trends indicate a specific hazard of tissue reaction to metal debris.
Product
Procotyl (Rim- Lock) Liners: REF PHA04702, REF PHA04704, REF PHA04706, REF PHA04708, REF PHA04710, REF PHA04712, REF PHA04714 For use with the conserve metal head
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0671-2017·2016-12-07
Baxter SIGMA Spectrum Infusion Pump Recall for Speaker Failure
Baxter is recalling SIGMA Spectrum Infusion Pumps to replace speakers that may fail prematurely, potentially affecting audible alarm tones.
Product
Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library, V8 Spectrum Infusion Pump, Product Code 35700BAX2, Unique Device Identifier GTIN 00085412091570, Rx ONLY -- Baxter Healthcare Corporation, Medina, NY 14103 --- NOTE: The speakers are a part of the rear case…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0664-2017·2016-12-07
Merge FlexConnect Software Recalled for Data Processing Errors
Merge Healthcare is recalling Merge FlexConnect software version 1.0 because communication protocols were not properly handled, preventing data from being processed by the LIS software.
Product
Merge FlexConnect software, a component of Merge LIS. Merge FlexConnect is middleware used in conjunction with Merge LIS to facilitate connection to external applications
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0155-2017·2016-12-07
Burel Recalls Hyolev MB Urinary Antiseptic Tablets Due to Manufacturing Deficiencies
Burel Pharmaceuticals is recalling 2,861 bottles of Hyolev MB Urinary Antiseptic Tablets due to manufacturing deviations that may cause assay or content uniformity failures.
Product
Hyolev MB URINARY ANTISEPTIC Tablets, Each tablet for oral administration contains: Hyoscyamine Sulfate 0.12 mg, Methenamine 81 mg, Methylene Blue 10.8 mg, Phenyl Salicylate 32.4 mg, Sodium Phosphate Monobasic 40.8 mg, 90 count bottles, Rx only, Manufactured for: BUREL…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0158-2017·2016-12-07
Burel Pharmaceuticals Recalls UROPHEN MB Urinary Antiseptic Tablets
Burel Pharmaceuticals is recalling UROPHEN MB Urinary Antiseptic Tablets due to manufacturing deviations that may cause assay or content uniformity failures.
Product
UROPHEN MB URINARY ANTISEPTIC Tablets, Each tablet contains: Methenamine 81.6 mg, Benzoic Acid 9.0 mg, Phenyl Salicylate 36 mg, Methylene Blue 10.8 mg, Hyoscyamine Sulfate 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0157-2017·2016-12-07
Burel Pharmaceuticals Recalls Uramit MB Urinary Antiseptic Capsules
Burel Pharmaceuticals is recalling Uramit MB Urinary Antiseptic Capsules due to manufacturing deviations that may cause assay or content uniformity failures.
Product
URAMIT MB URINARY ANTISEPTIC Capsules, Each capsule contains: Methenamine 118 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue 10 mg, Hyoscyamine Sulfate, 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0675-2017·2016-12-07
Teleflex Recalls Arrow OnControl Bone Marrow Biopsy System Trays
Teleflex Medical is recalling 113,647 units of Arrow OnControl Bone Marrow Biopsy System Trays due to a potential incomplete seal on the outer sterile package.
Product
ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow¿ OnControl Bone Marrow…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0168-2017·2016-12-07
Nationwide Laboratories Recalls Phenazopyridine Hydrochloride Tablets Due to CGMP Deviations
Nationwide Laboratories LLC is recalling Phenazopyridine Hydrochloride Tablets, 200 mg, due to manufacturing deviations that may result in assay or content uniformity failures.
Product
Phenazopyridine Hydrochloride Tablets, USP, 200 mg, 100 count bottles, Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830, NDC 42937-702-10.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0161-2017·2016-12-07
Burel Pharmaceuticals Recalls Phenazopyridine Hydrochloride Tablets Due to CGMP Deviations
Burel Pharmaceuticals is recalling 17,788 bottles of Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may cause assay or content uniformity failures.
Product
Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only, Manufactured for: Burel Pharmaceuticals, Inc., Richland, MS --- NDC 35573-304-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0670-2017·2016-12-07
Baxter Recalls Sigma Spectrum Infusion Pumps Due to Speaker Failure Risk
Baxter Healthcare is recalling 5,976 Sigma Spectrum Infusion Pumps because some speakers may fail prematurely, potentially affecting audible alarms.
Product
sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library, V6 Spectrum Infusion Pump, Product Code 35700BAX and 35700BAXR, Unique Device Identifier GTIN 00085412091570, Rx ONLY -- Sigma, LLC Medina, NY 14103 --- NOTE: The speakers are a part of the rear case assembly…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0160-2017·2016-12-07
Burel Pharmaceuticals Recalls Indiomin MB Capsules Due to Manufacturing Deficiencies
Burel Pharmaceuticals is recalling 795 bottles of Indiomin MB capsules due to manufacturing deviations that may cause assay or content uniformity failures.
Product
Indiomin MB URINARY ANTISEPTIC, ANTISPASMODIC Capsules, Each capsule contains: Methenamine 120 mg, Monobasic Sodium Phosphate 40.8 mg, Methylene Blue, 10 mg; Hyoscyamine Sulfate, 0.12 mg, 100 count, Rx only, Manufactured for: BUREL PHARMACEUTICALS, NDC 35573-315-10
Category
Drug
Distribution
Distributed nationwide