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.

57776–57800 of 73856

HighFDA (Devices)·Z-1990-2014·2014-07-09
Siemens MicroScan WalkAway Plus Instruments Recalled for Hinge Spring Failure
Siemens is recalling MicroScan WalkAway-40 and 96 plus instruments because springs in the access door hinge assembly are detaching, causing premature failure and potential safety issues.
Product
MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus instrument access door hinge. Siemens Healthcare Diagnostics, Inc. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2052-2014·2014-07-09
Savor Brands Large Pitted Kalamata Olives Recalled Due to Glass Contamination
Dot Foods Inc. is voluntarily recalling Savor Brands Large Pitted Kalamata Olives because they may contain glass.
Product
Large Pitted Kalamata Olives, packaged in 4.4lb black plastic barrels. Labeling reads in part: Savor Greek Large Pitted Kalamata Olives, refrigerate after opening, these olives are mechanically pitted and may contain pit fragments, DR WT 4.4LBS (2kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1976-2014·2014-07-09
Integra LED Battery Charger Recalled for Premature Failure
Integra LifeSciences is recalling 1,250 LED battery chargers because they may fail prematurely and not charge the LED battery as intended.
Product
Integra¿ LED Battery Charger, Single Bay. Product Number: 90523 The LED Headlight System Battery Charger (90523) is an accessory to the LED Headlight System: 90520US - LED Headlight w/Battery & AC/DC Power Supply - US 90520EU - LED Headlight w/Battery & AC/DC Power…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1960-2014·2014-07-09
Siemens ADVIA Centaur HCY Diluent Recalled for Inaccurate Dilution Recovery
Siemens Healthcare Diagnostics is recalling ADVIA Centaur HCY Diluent because dilution recovery was lower than reported in the instructions for use.
Product
ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533), SMN 10310370, and Ancillary Pack Catalog number 03302138 (124581), SMN 10378677. Used on the ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP platforms. For in vitro diagnostic use in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1938-2014·2014-07-09
Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues
Zimmer is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 7. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1939-2014·2014-07-09
Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues
Zimmer, Inc. is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 8. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1936-2014·2014-07-09
Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues
Zimmer, Inc. is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 5. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1966-2014·2014-07-09
Intuitive Surgical Recalls da Vinci Vision Troubleshooting Guides
Intuitive Surgical is recalling Vision Troubleshooting Guides for the da Vinci Surgical System to remove references to the Emergency Grip Release Wrench.
Product
Vision Troubleshooting Guide for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1964-2014·2014-07-09
Intuitive Surgical Recalls da Vinci System Manuals Due to Wrench Removal
Intuitive Surgical is recalling da Vinci Surgical System manuals and guides to remove references to the Emergency Grip Release Wrench.
Product
System Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2061-2014·2014-07-09
National Vitamin Recalls Ferrous Gluconate Tablets Due to Mislabeled Iron Content
National Vitamin Co Inc is recalling Nature's Blend Ferrous Gluconate Tablets because the front panel incorrectly lists 65 mg of elemental iron instead of the correct 36 mg.
Product
Ferrous Gluconate Tablets, 5gr (325 mg), Elemental Iron 36 mg, 100 Tablets, UPC 0 79854 50032 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1415-2014·2014-07-09
Caraco Recalls Venlafaxine Hydrochloride Extended-Release Tablets for Dissolution Failures
Caraco Pharmaceutical Laboratories is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Tablets, 150 mg, because stability results showed the product did not meet drug dissolution specifications.
Product
Venlafaxine Hydrochloride Extended-Release Tablets, 150 mg, Rx only, Packaged in 30 Count and 90 Count Bottles. Distributed by: Caraco Pharmaceutical Laboratories, Ltd., 1150 Elijah McCoy Drive, Detroit, MI 48202; Manufactured at: Sun Pharmaceutical Ind. Ltd., Halol-Baroda…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1967-2014·2014-07-09
Intuitive Surgical Recalls da Vinci Surgical System Instrument Release Kits
Intuitive Surgical is recalling Instrument Release Kits for the da Vinci Surgical System to remove the Emergency Grip Release Wrench.
Product
Insert for IRK for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1965-2014·2014-07-09
Intuitive Surgical Recalls da Vinci Endowrist Instrument Manuals
Intuitive Surgical is recalling Endowrist Instrument and Accessory Manuals for the da Vinci Surgical System to remove the Emergency Grip Release Wrench.
Product
Endowrist Instrument and Accessory Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1984-2014·2014-07-09
Synthes B37 Replacement Screws Recalled for Potential Mislabeling
Synthes, Inc. is recalling 44 B37 Replacement Screws because the package may not contain the screws identified on the label.
Product
Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming arm, part numbers 3.113.025 and 03.113.026. Surgical instrument for use with Low Bend Medial Distal Tibia Plate. Orthopedic.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1980-2014·2014-07-09
Nidek AFC-330 Fundus Camera Recalled for Image Defects
Nidek Inc. is recalling 185 AFC-330 Non-Mydriatic Auto Fundus Cameras because images may contain white spots that could affect diagnosis.
Product
Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for use in capturing images of the retina and anterior segment of the eye. Distributed by Nidek, Inc, and Marco Opthalmic Inc. Manufactured by Nidek Co. Ltd, Japan.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1958-2014·2014-07-09
Focus Diagnostics Recalls Simplexa Flu A/B & RSV Direct Assay Kits
Focus Diagnostics is correcting labeling for 614 Simplexa Flu A/B & RSV Direct kits due to sporadic false signals that may increase false results.
Product
Simplexa" Flu A/B & RSV Direct, Model Number: MOL2650. 510(k) K120413 Simplexa" Flu A/B & RSV Direct. The Focus Diagnostics Simplexa Flu A/B & RSV Direct assay is intended for use on the 3M Integrated Cycler instrument for the in vitro qualitative detection and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1412-2014·2014-07-09
Forest Pharmaceuticals Recalls Bystolic Tablets for Dissolution Failure
Forest Pharmaceuticals is recalling Bystolic (nebivolol) 20 mg tablets because they failed stage III dissolution testing. The recall affects 92,544 bottles distributed nationwide.
Product
Bystolic (nebivolol) tablets, 20 mg/tablet. 7 Tablet Professional Sample Bottle, Rx Only. Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, Missouri 63045. NDC 0456-1420-07.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2054-2014·2014-07-09
Physique Enhancing Science Recalls ALPHAMINE Powder Due to Unapproved Ingredient
Physique Enhancing Science is recalling ALPHAMINE thermogenic powder because it contains Aegeline, an unapproved new dietary ingredient.
Product
Physique Enhancing Science ALPHAMINE, Powerful Thermogenic Powder, DIETARY SUPPLEMENT Net Wt. 8.9 oz (252 g). Raspberry Lemonade and Fruit Punch flavors.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1969-2014·2014-07-09
Intuitive Surgical Recalls Vessel Sealer Addendum for da Vinci Systems
Intuitive Surgical is recalling Vessel Sealer Addendum software for da Vinci surgical systems to update user manuals and remove the Emergency Grip Release Wrench.
Product
Vessel Sealer Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1946-2014·2014-07-09
Origio Pasteur Pipets Recalled Due to Packaging Sterility Breach
Origio, Inc. is recalling Pasteur Pipets used in IVF laboratories because a breach in the nylon pouch sterile barrier was identified.
Product
Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model numbers: PP-5.75-90 PP-9-90 PP-5.75-90PL PP-9-90PL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1932-2014·2014-07-09
Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues
Zimmer is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 2. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1971-2014·2014-07-09
Intuitive Surgical Recalls da Vinci Manuals Due to Wrench Removal
Intuitive Surgical is recalling da Vinci Surgical System manuals to remove the Emergency Grip Release Wrench from the documentation.
Product
Single Site US Manuals and Single Site OUS Manuals for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1934-2014·2014-07-09
Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues
Zimmer, Inc. is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 4. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1933-2014·2014-07-09
Zimmer Recalls NexGen Knee Components Due to Thread Specification Issues
Zimmer, Inc. is voluntarily recalling specific lots of NexGen Complete Knee Solution stemmed tibial components because the threads may be out of specification.
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 3. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1975-2014·2014-07-09
Intuitive Surgical Recalls da Vinci Surgical System Quick Reference Guides
Intuitive Surgical is recalling Natural Rubber Latex Quick Reference Guides for the da Vinci Surgical System to update documentation and remove a specific wrench part.
Product
Natural Rubber Latex QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.
Category
Medical Device
Distribution
Distributed nationwide