State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52976–53000 of 73847

ModerateFDA (Drugs)·D-1215-2015·2015-07-15
Apotex Recalls Enalapril Maleate and Hydrochlorothiazide Tablets for Uniformity Issues
Apotex Inc. is recalling 4,584 bottles of Enalapril maleate and hydrochlorothiazide tablets, 10/25 mg, because the product may not meet blend uniformity specifications.
Product
Enalapril maleate and hydrochlorothiazide tablets USP, 10/25 mg, 100-count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private Limited, Plot 1 & 2, Bommasandra Industrial Area, 4th Phase Jigani Link Road, Bangalore, Karnataka…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2005-2015·2015-07-15
Stradis Breast Augmentation Kits Recalled Due to Component Recall
Stradis Healthcare is recalling breast augmentation kits because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.
Product
Breast Augmentation Pack and Breast Augmentation Expanded Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2035-2015·2015-07-15
Stradis Face Lift Pack Recalled Due to Component Defect
Stradis Healthcare is recalling Face Lift Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Product
Face Lift Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2000-2015·2015-07-15
Stradis Healthcare Recalls Lipo/Buttocks Surgical Packs Due to Component Recall
Stradis Healthcare is recalling Lipo/Buttocks Packs because they contain a Devon Light Glove component that Medtronic is recalling.
Product
Lipo/Buttocks Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2011-2015·2015-07-15
Stradis Suction Pack Recalled Due to Component Recall by Medtronic
Stradis Healthcare is recalling Suction Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.
Product
Suction Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1212-2015·2015-07-15
Apotex Recalls Losartan Potassium Tablets Due to Uniformity Issues
Apotex Inc. is recalling Losartan potassium tablets 25 mg because they may not meet blend uniformity specifications. The recall covers 45,708 bottles distributed nationwide, in Hawaii, and Puerto Rico.
Product
Losartan potassium tablets USP, 25 mg, 90- count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private Limited, Plot 1 & 2, Bommasandra Industrial Area, 4th Phase Jigani Link Road, Bangalore, Karnataka, 560099, India NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2032-2015·2015-07-15
Stradis Cysto Pack Recalled Due to Component Recall by Medtronic
Stradis Healthcare is recalling Cysto Packs because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.
Product
Cysto Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1221-2015·2015-07-15
American Health Packaging Recalls Azithromycin Tablets Due to CGMP Deviations
American Health Packaging is recalling specific lots of Azithromycin tablets because the firm did not adequately investigate customer complaints.
Product
Azithromycin tablets, USP 500mg, packaged in 10-count blisters (NDC 68084-279-11); 3 blister packs per carton (NDC 68084-279-21); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1222-2015·2015-07-15
American Health Packaging Recalls Azithromycin Tablets Due to Complaint Investigation Failures
American Health Packaging is recalling 838 cartons of Azithromycin 600mg tablets because the firm did not adequately investigate customer complaints.
Product
Azithromycin tablets, USP 600mg, packaged in 10-count blisters (NDC 68084-464-11); 3 blister packs per carton (NDC 68084-464-21); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1997-2015·2015-07-15
Stradis Healthcare Recalls Phleb Packs Containing Recalled Devon Light Gloves
Stradis Healthcare is recalling Phleb Packs and Laser Phleb Packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall.
Product
Phleb Pack and Laser Phleb Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1999-2015·2015-07-15
Stradis Healthcare Recalls Lipo Packs Containing Recalled Devon Light Gloves
Stradis Healthcare is recalling Lipo Packs, Expended Packs, and Trays because they contain Devon Light Gloves that Medtronic is recalling.
Product
Lipo Pack, Liposuction Expended Pack, and Liposuction Tray - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1223-2015·2015-07-15
American Health Packaging Recalls Azithromycin Tablets Due to CGMP Deviations
American Health Packaging is recalling 2,068 cartons of Azithromycin tablets 250mg due to inadequate investigation of customer complaints.
Product
Azithromycin tablets, USP 250mg, packaged in 10-count blisters (NDC 68084-278-11); 10 blister packs per carton (NDC 68084-278-01); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2027-2015·2015-07-15
Stradis ENT Packs Recalled Due to Medtronic Glove Component Recall
Stradis Healthcare is recalling ENT Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Product
ENT Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2026-2015·2015-07-15
Stradis Healthcare Recalls Knee Arthro Packs Due to Component Recall
Stradis Healthcare is recalling Knee Arthro Packs because they contain a Devon Light Glove component that Medtronic is recalling.
Product
Knee Arthro Pack and Knee Arthro Pack II - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2010-2015·2015-07-15
Stradis Plastic Packs Recalled Due to Medtronic Component Recall
Stradis Healthcare is recalling Plastic Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.
Product
Plastic Pack and Plastic HNP Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2040-2015·2015-07-15
Stradis Orthopedic Split Drape Pack Recalled Due to Component Issue
Stradis Healthcare is recalling Orthopedic Split Drape Packs because they contain a Devon Light Glove component recalled by Medtronic.
Product
Orthopedic Split Drape Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2033-2015·2015-07-15
Stradis Healthcare Recalls Surgical Convenience Kits Containing Recalled Devon Light Gloves
Stradis Healthcare is recalling surgical convenience kits because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
Product
Open Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1998-2015·2015-07-15
Stradis Standard Pack Recalled Due to Medtronic Component Recall
Stradis Healthcare is recalling Standard Packs containing Devon Light Gloves because the glove component was recalled by Medtronic.
Product
Standard Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2028-2015·2015-07-15
Stradis Hand Pack Recall Due to Medtronic Glove Component Issue
Stradis Healthcare is recalling Hand Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.
Product
Hand Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2018-2015·2015-07-15
Stradis Face Neck Pack Recalled Due to Component Defect
Stradis Healthcare is recalling Face Neck Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Product
Face Neck Pack - contains Devon Light Glove Used during surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2056-2015·2015-07-15
Integra Recalls Tuohy Needles Due to Incorrect Gauge and Length Labeling
Integra LifeSciences is voluntarily recalling 123 Tuohy needles because they were incorrectly labeled as 18 gauge, 3.5 inch instead of 20 gauge, 5 inch.
Product
Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle), 20 gauge x 5 inch. Plastic Hub, Metal Stylet, calibrations (10BX). Integra¿ Long Epidural Steroid Injection Needle (Catalogue #PITRW2050). Peel Pouch. The Integra¿ Long Epidural Steroid Injection Needle is packaged…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2049-2015·2015-07-15
Bard Access Systems Recalls PowerPICC Solo Catheters for Labeling Errors
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels display incorrect expiration dates.
Product
PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Nurse Full Tray with Microintroducer (with Lidocain) The PowerPICC Solo catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2048-2015·2015-07-15
Bard Access Systems Recalls PowerPICC Solo Catheter Kits for Labeling Errors
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because they have incorrect expiration dates on the primary labeling.
Product
PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Barrier Tray with Microintroducer The PowerPICC Solo catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2050-2015·2015-07-15
Bard Access Systems Recalls PowerPICC Solo Catheter Kits for Labeling Errors
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels contain incorrect expiration dates.
Product
PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer (Single-Lumen) (Sherlock) The PowerPICC Solo catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2047-2015·2015-07-15
Bard Access Systems Recalls PowerPICC Solo Catheter Kits for Labeling Errors
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels contain incorrect expiration dates.
Product
PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal Barrier Tray with Microintroducer The PowerPICC Solo catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide