State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53876–53900 of 73850

SevereFDA (Drugs)·D-0973-2015·2015-05-06
Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization
Hospira is voluntarily recalling specific lots of Ketorolac Tromethamine Injections because of crystallization. The affected products were distributed nationwide, in Puerto Rico, and in Guam.
Product
Ketorolac Tromethamine Inj. USP, 60 mg (30 mg/mL), 2 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3796-01 --- Also labeled under NOVAPLUS label NDC 00409-3796-49
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2090-2015·2015-05-06
Navajo Pride Flour Recalled for Salmonella Contamination
Navajo Agricultural Products Industry is recalling Navajo Pride Bleached All Purpose Flour due to Salmonella contamination.
Product
Navajo Pride Bleached All Purpose Flour in 50 lb, 25 lb, and 5 lb Cloth Bags by Navajo Agricultural Products Industry.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2084-2015·2015-05-06
Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Contamination
Sabra Dipping Company is recalling 32-ounce containers of Classic Hummus without Garnish after a sample tested positive for Listeria monocytogenes.
Product
Sabra Classic Hummus without Garnish 32oz UPC 040822342049 / 301216 Sabra Dipping Co. LLC, White Plains, NY
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2085-2015·2015-05-06
Sabra Classic Hummus Recalled Due to Listeria Monocytogenes Contamination
Sabra Dipping Company is recalling Sabra Classic Hummus after a sample tested positive for Listeria monocytogenes. The product was distributed nationwide.
Product
Sabra Classic Hummus, 17oz Six Pack UPC 040822017497 / 301290 Sabra Dipping Co. LLC, White Plains, NY
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2086-2015·2015-05-06
Sabra Hummus Recalled Due to Listeria Monocytogenes Contamination
Sabra Dipping Company is recalling specific tubs of Roasted Garlic and Classic Hummus after a Michigan sample tested positive for Listeria monocytogenes.
Product
Sabra Roasted Garlic Hummus, Classic Hummus packed in 2/23.5 oz plastic tub/package. UPC 040822342209, Sabra Dipping Co. LLC, White Plains, NY
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2076-2015·2015-05-06
Hope Foods Recalls Kale Pesto Hummus for Undeclared Walnuts
Hope Foods is voluntarily recalling one lot of Kale Pesto Hummus because it contains undeclared walnuts. Consumers should check for the specific lot code and UPC.
Product
Organic Hummus HOPE Kale Pesto Spread Good Things, Net Wr 8 oz (227g), Best By date of 05/04/15.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0971-2015·2015-05-06
Teva Recalls Fluoxetine Capsules Due to Residual Solvent Impurity
Teva Pharmaceuticals USA is recalling specific lots of Fluoxetine Capsules USP, 20 mg, due to an elevated level of a residual solvent impurity in the active pharmaceutical ingredient.
Product
FLUOXETINE — FLUOXETINE (FLUOXETINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1548-2015·2015-05-06
Dako Omnis Software Module Recalled for Test Request Errors
Dako North America is recalling the Test Request Distributor software module for the Dako Omnis System because it may execute the wrong test after a user updates a request.
Product
Test Request Distributor (TRD 1.3 and TRD 1.4), a software module used on the Dako Omnis System, an automated slide stainer for in vitro diagnostic use. The TRD is intended to distribute patient case, appropriate parts information, track changes, and transform test…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2096-2015·2015-05-06
Cuisine Innovations Recalls Black Bean Burgers for Undeclared Peanut
Cuisine Innovations is recalling Black Bean Burgers because they may contain undeclared peanut protein. The product was distributed nationwide.
Product
Black Bean Burger 4.5 oz 40 pieces Net Wt. 11.25 lbs. (5.10 kg)Manufactured by: Cuisine Innovations, LLC Lakewood, NJ 08701 USA UPC 00030499640296 For Institutional Use Only
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1556-2015·2015-05-06
CareFusion LightWand Stylet Recalled for Sterile Packaging Breach Risk
Vital Signs Colorado is recalling LightWand Stylets because sterile packaging may be breached without visible signs, posing a patient safety risk.
Product
CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1519-2015·2015-05-06
Lumenis Light Sheer Desire Diode Laser System Recalled for Software Error
Lumenis is recalling 117 Light Sheer Desire Diode Laser Systems because software parameters exceed manual settings, potentially causing burns.
Product
Light Sheer Desire Diode Laser System with XC Handpiece Accessory options.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·Ff-2095-201·2015-05-06
Guiltless Gourmet Southwestern Veggie Burger Recalled for Undeclared Peanut
Cuisine Innovations is recalling Guiltless Gourmet Southwestern Veggie Burgers because they may contain undeclared peanut protein.
Product
Guiltless Gourmet Southwestern Veggie Burger 2.5oz 48 pieces Distributed by: Cuisine Innovations, LLC. 1920 Swarthmore Avenue, Lakewood, NJ 08701 USA UPC 00030499503256 For institutional use only
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2015·2015-05-06
Synthes Small Battery Drive Oscillating Saw Attachment Recall
The Anspach Effort, Inc. is recalling Synthes Small Battery Drive Oscillating Saw Attachments because they may disengage during surgery, posing a risk of injury.
Product
Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1559-2015·2015-05-06
Steris Caviwave Pro Ultrasonic Cleaning System Recalled for Power Failure Risk
Steris is recalling 491 Caviwave Pro Ultrasonic Cleaning Systems because a power interruption may stop the pump and generator without alerting the user.
Product
Caviwave Pro Ultrasonic Cleaning System, Product Usage: To wash (remove tissue, blood and other contaminants) or dry laparoscopic and general surgical instruments prior to final disinfection and sterilization as required.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2097-2015·2015-05-06
Bon Appetizers Southwestern Veggie Burgers Recalled for Undeclared Peanut
Cuisine Innovations LLC is recalling Southwestern Veggie Burgers because they may contain undeclared peanut protein.
Product
Southwestern 4oz Veggie Burger 36 count Net Wt 9 lb. (4.08 kg) Distributed by Performance Food Group Richmond, VA 23238 UPC 00806795422276
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2098-2015·2015-05-06
Chef's Line Black Bean Burger Recalled for Undeclared Peanut
Cuisine Innovations LLC is recalling Chef's Line Black Bean Burgers because they may contain undeclared peanut protein.
Product
Chef's Line Black Bean Burger 36-4.25 oz Net Wt. 9 Lb 9 oz. (4.33 kg) Distributed by US Foods, Inc. Rosemont, IL 60018 UPC 50758108685357
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1557-2015·2015-05-06
Vital Signs LightWand Stylet Recalled for Sterile Packaging Breach
Vital Signs Colorado is recalling LightWand Stylets because sterile packaging may be breached without visible signs, posing a patient safety risk.
Product
Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1542-2015·2015-05-06
Spacelabs Ultraview SL Command Modules Recalled for Monitoring Suspension
Spacelabs is recalling Ultraview SL Command Modules upgraded with the Masimo SpO2 Option because monitoring suspends for approximately 10 seconds during resets.
Product
Ultraview SL Command Modules, Model 91496-M, upgraded with the Masimo SpO2 Option. Product Usage: The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various clinical parameters from an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1520-2015·2015-05-06
AmTryke Model 1424 Hand Cycle Recalled for Cracked Frames
Amtryke LLC is recalling 53 Model 1424 Community Cruiser Hand Cycles due to complaints of cracked frames. The recall covers units distributed nationwide to 18 states.
Product
AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1552-2015·2015-05-06
Fresenius 2008K2 Hemodialysis Machines Recalled for Acetate Display Error
Fresenius Medical Care is recalling 2008K2 hemodialysis machines because the GranuFlo acetate value is incorrectly displayed as 4mEq/l instead of 8mEq/l on the Select Concentrate screen.
Product
2008 Series Hemodialysis Machines: 2008K2 with the following product code and description: 190633 2008K2 HEMO SYSTEM, OPTIONAL MODULE; 190618 2008K2 HEMODIALYSIS SYS OLC/DP, SPANISH; 190610 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS; 190630 2008K2 MACHINE, SHORT CAB, OLC/DP, HP…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1529-2015·2015-05-06
Beckman Coulter Recalls MicroScan Panels Due to Performance Limitation
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin omitted a performance limitation for Proteus mirabilis.
Product
MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels Containing Lower Imipenem Dilutions for Reporting CLSI M100-S20 Breakpoints Panel: Neg/BP Combo 47, Catalog B1017-417 Microbiology: For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0972-2015·2015-05-06
Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization
Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection due to crystallization. The recall covers products distributed nationwide, in Puerto Rico, and in Guam.
Product
Ketorolac Tromethamine Inj. USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3795-01--- Also labeled under NOVAPLUS label NDC 00409-3795-49
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1527-2015·2015-05-06
MedComp Recalls 9F Plastic Dual Port Vascular Access Devices
Medical Components, Inc. is recalling 325 units of 9F Plastic Dual Port vascular access devices because they were not covered under FDA clearance.
Product
9F Plastic Dual Port; The port systems are totally implantable vascular access devices. They consist of an injection port, a self-sealing membrane and a detachable catheter. The port systems provide repeated vascular access and are applicable for delivery of: medications…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0970-2015·2015-05-06
Teva Recalls Fluoxetine Capsules Due to Residual Solvent Impurity
Teva Pharmaceuticals USA is recalling specific lots of Fluoxetine Capsules 10 mg due to an elevated level of a residual solvent impurity in the active ingredient.
Product
FLUOXETINE — FLUOXETINE (FLUOXETINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1528-2015·2015-05-06
Beckman Coulter MicroScan Panels Recalled for Missing Proteus Performance Warning
Beckman Coulter is recalling MicroScan Dried Gram Negative MIC/Combo Panels because a technical bulletin failed to mention performance limitations for Proteus mirabilis.
Product
MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels Containing Lower Imipenem Dilutions for Reporting CLSI M100-S20 Breakpoints Panel: Neg Combo 50, Catalog B1017-406 Microbiology: For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried Gram…
Category
Medical Device
Distribution
Distributed nationwide