State

Northern Mariana Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36001–36025 of 73760

HighFDA (Devices)·Z-0409-2019·2018-11-14
Siemens Dimension Thermal Chamber Motor Cable Recall for Insulation Defect
Siemens is recalling 277 Dimension thermal chamber motor cables worldwide due to single insulation instead of required double insulation, posing a potential electrical shock risk.
Product
Dimension Thermal Chamber Motor Cable located in the following models: Model/UDI Number: Dimension¿ EXL 200 00630414593579; Dimension¿ EXL with LM 00630414593500; Dimension¿ EXL with LM with STM 00630414593593; Dimension¿ RxL Max 00630414949789; Dimension¿ RxL Max HM…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0393-2019·2018-11-14
Zimmer Biomet Recalls RapidFlap SpinDown Clamp Due to Assembly Error
Zimmer Biomet is recalling 12,825 units of the RapidFlap System 12mm SpinDown Clamp because the nut was assembled incorrectly. The defect affects sterile clamps used for craniotomy bone flap re-attachment.
Product
Biomet Microfixation RapidFlap System 12mm SpinDown Clamp, sterile Ref Number: 75-1020 Used for the re-attachment of the bone flap after a craniotomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0228-2019·2018-11-14
Qualgen Recalls Estradiol Pellets Due to Sterility Assurance Concerns
Qualgen, LLC is recalling Estradiol 18mg pellets because the company cannot assure the sterility of the product. The recall covers specific vial sizes distributed nationwide.
Product
Estradiol 18mg pellet, 1 count (NDC 69761-018-01), 6 count (NDC 69761-018-06), 12 count (NDC 69761-018-12), and 30 count (NDC 69761-018-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0387-2019·2018-11-14
Becton Dickinson Recalls PCEA Administration Sets Due to Potential Leaks
Becton Dickinson is recalling PCEA Administration Sets because they may leak at the connection point. The recall covers 566,737 units distributed worldwide.
Product
PCEA Kit ASV Yellow Stripe Microbore, Catalog Number 10800177 Product Usage: PCEA Administration Set. Microbore tubing with Yellow Identification Stripe. Anti-siphon valve. Set cannot be used for gravity infusion 1. Connect PCA syringe to female luer on administration set.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0383-2019·2018-11-14
Request Foods Recalls Evol Butternut Squash Lasagna Due to Contamination Risk
Request Foods Incorporated is recalling Evol Butternut Squash Lasagna because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Evol Butternut Squash Lasagna 10.8oz. UPC 91627 00794 Frozen 8, 10.8oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0385-2019·2018-11-14
Request Foods Recalls Kashi Chimichurri Quinoa Bowls for Listeria and Salmonella
Request Foods Incorporated is recalling Kashi Chimichurri Quinoa Bowls because ingredients were possibly contaminated with Listeria monocytogenes and Salmonella.
Product
Kashi,Chimichurri Quinoa Bowl 9oz. UPC 18627 10440 Frozen 8, 9oz. units per case
Category
Food
Distribution
Distributed nationwide
HighNHTSA·18V803000·2018-11-14
Volkswagen and Audi Recall 2018 Models for Rear Seat Weld Defect
Volkswagen and Audi are recalling 2018 e-Golf, Golf R, A3, and RS3 vehicles because incorrectly welded rear seat head restraint guide sleeves may reduce stability in a crash.
Product
AUDI — AUDI, VOLKSWAGEN A3 CABRIOLET, GOLF R, RS 3, E-GOLF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0395-2019·2018-11-14
Request Foods Recalls Jenny Craig Butternut Squash Ravioli for Contamination
Request Foods Incorporated is recalling Jenny Craig Butternut Squash Ravioli because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Jenny Craig Butternut Squash Ravioli 7.5oz. UPC 55447 00625 Frozen 30, 7.5oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0373-2019·2018-11-14
Howmedica Recalls 15 Pouches of Sterile Knee Instruments Due to Barrier Risk
Howmedica Osteonics Corp. is recalling 15 pouches of sterile knee instruments because the outer sterile barrier may be compromised.
Product
Sterile Knee Instruments Disposable Fluted Headless Pins, DIA 3.2mm LNTH 89mm, REF 7650-2038A - Product Usage: Howmedica Osteonics Corp. (Stryker, Joint Reconstructive Division) Sterile Instrumentation consists of manual surgical instrumentation intended for use during hip…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0393-2019·2018-11-14
Request Foods Recalls Moe's Southwest Vegetarian Breakfast Bowls
Request Foods Incorporated is recalling Moe's Southwest Vegetarian Breakfast Bowls due to possible contamination with Listeria monocytogenes and Salmonella.
Product
Moe's Southwest Vegetarian Breakfast Bowl 8oz. UPC 38000 17240 Frozen 8, 8oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0378-2019·2018-11-14
Request Foods Recalls Evol Portabella Goat Cheese Ravioli for Contamination Risk
Request Foods Incorporated is recalling Evol Portabella Goat Cheese Ravioli because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Evol Portabella Goat Cheese Ravioli 18oz UPC 91627 00789 Frozen 4, 18oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0394-2019·2018-11-14
Request Foods Recalls Roasted Vegetable Lasagna Due to Listeria and Salmonella Risk
Request Foods Incorporated is recalling PC President's Choice Roasted Vegetable Lasagna because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
PC Presidents Choice Roasted Vegetable Lasagna 1.13kg. UPC 60383 75647 Frozen 12 units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0399-2019·2018-11-14
Request Foods Recalls Tropical Bowl with Barramundi for Listeria and Salmonella Risk
Request Foods Incorporated is recalling Love The Wild Hawaiian Style Tropical Bowl with Barramundi because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Love The Wild Hawaiian Style Tropical Bowl with Barramundi 9oz. UPC 50068 00602 Frozen 6, 9oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0379-2019·2018-11-14
El Monterey Cheese Enchiladas Recalled Due to Possible Listeria and Salmonella Contamination
The FDA is recalling El Monterey Cheese Enchiladas because suppliers reported possible contamination with Listeria monocytogenes and Salmonella bacteria.
Product
El Monterey Cheese Enchilada 10 oz. UPC 71007 31810 Frozen 8, 10oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0381-2019·2018-11-14
Request Foods Recalls Udi's Broccoli & Kale Lasagna Due to Contamination Risk
Request Foods Incorporated is recalling Udi's Broccoli & Kale Lasagna because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Udi's, Broccoli & Kale Lasagna 8 oz. UPC 98997 80801 Frozen 6, 8oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0402-2019·2018-11-14
Request Foods Recalls Beecher's Enchilada Bowls for Listeria and Salmonella
Request Foods Incorporated is recalling Beecher's Enchilada Bowl Rojo due to potential contamination with Listeria monocytogenes and Salmonella.
Product
Beecher's Enchilada Bowl Rojo 9oz. UPC 82045 11380 Frozen 8, 9oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0386-2019·2018-11-14
Becton Dickinson Recalls PCEA ASV Yellow Microbore Administration Sets
Becton Dickinson is recalling PCEA ASV Yellow Microbore administration sets because they may leak at the luer lock connection.
Product
PCEA ASV Yellow Microbore, Catalog Numbers 30893, 30893-07 Product Usage: PCEA Administration Set. Microbore tubing with Yellow Identification Stripe. Anti-siphon valve. Set cannot be used for gravity infusion 1. Connect PCA syringe to female luer on administration set. 2.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0394-2019·2018-11-14
Zimmer Biomet Recalls RapidFlap SpinDown Clamps Due to Assembly Error
Zimmer Biomet is recalling RapidFlap SpinDown Clamps because the nut was assembled incorrectly. The defect affects 11,736 units distributed worldwide.
Product
Biomet Microfixation RapidFlap System, 12MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1020-12 Used for the re-attachment of the bone flap after a craniotomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0375-2019·2018-11-14
Request Foods Recalls Evol Butternut Squash Ravioli for Contamination
Request Foods Incorporated is recalling Evol Butternut Squash & Sage Ravioli because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Evol Butternut Squash & Sage Ravioli 18oz. UPC 91627 00776 Frozen 4, 18oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0387-2019·2018-11-14
Request Foods Recalls Kashi Black Bean Mango Bowls for Contamination
Request Foods Incorporated is recalling Kashi Black Bean Mango Bowls because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Kashi, Black Bean Mango Bowl 10oz. UPC 18627 10607 Frozen 8, 10oz. units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0379-2019·2018-11-14
AROA Endoform Dermal Template Recalled for Potential Pouch Seal Failure
AROA Biosurgery is recalling 8,853 boxes of Endoform Dermal Template 4x5 due to a potential for pouch seal failure.
Product
Endoform Dermal Template 4x5, SKU 529313 Product Usage: Endoform Dermal Template is a sterile, single use ovine forestomach derived extracellular matrix intended to cover, protect and provide a moist wound environment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0396-2019·2018-11-14
Jenny Craig Butternut Squash Ravioli Recalled for Listeria and Salmonella Risk
Request Foods Incorporated is recalling Jenny Craig Butternut Squash Ravioli because ingredients may be contaminated with Listeria monocytogenes and Salmonella.
Product
Jenny Craig Butternut Squash Ravioli 213g. UPC 55447 10625 Frozen 30, 213g. units per case
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0399-2019·2018-11-14
Zimmer Biomet Recalls StageOne Hip Cement Spacer Molds
Zimmer Biomet is recalling 72 units of StageOne Hip cement spacer molds due to a potential for comingling of 43MM and 51MM sizes.
Product
StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds are sterile disposables made of medical grade silicone with a 316L stainless steel reinforcement stem. They are designed to be filled with polymethylmethacrylate/gentamicin bone…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0222-2019·2018-11-14
Baxter Recalls Metoprolol Tartrate Injection Due to pH Specification Failures
Baxter Healthcare is recalling 402,165 vials of Metoprolol Tartrate Injection because the solution's pH shifted upward during shelf life.
Product
METOPROLOL — METOPROLOL (METOPROLOL TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0218-2019·2018-11-14
Janssen Recalls Ortho-Novum 7/7/7 Tablets Due to Incorrect Dispenser Instructions
Janssen Pharmaceuticals is recalling Ortho-Novum 7/7/7 tablets because the packaging included instructions for the wrong type of pill dispenser.
Product
Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets, 0.5 mg/0.035 mg, 0.75 mg/0.035 mg, 1 mg/0.035, 28-Day Regimen per pouch, packaged in a) 6 Veridate Tablet Dispensers and 6 Refill pouches (NDC 504-58-178-28) per carton (NDC 50458-178-06); and b) 12 Veridate Tablet…
Category
Drug
Distribution
Distributed nationwide