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.

35276–35300 of 73760

SevereFDA (Drugs)·D-0470-2019·2019-02-20
Promise Pharmacy Recalls Myer's Cocktail Vials Due to Sterility Concerns
Promise Pharmacy is recalling 5 vials of Myer's Cocktail due to a lack of sterility assurance. The product was distributed nationwide.
Product
Myer's Cocktail, Pyridoxine/Dexpanthenol/Calcium Gluconate/Niacinamide/Vit B6/Vit B1/Leucine/Vit B5/Riboflavin/Ascorbic Acid/Hydroxycobalamin/Magnesium Chloride, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0464-2019·2019-02-20
Promise Pharmacy Recalls IGF-1-LR3 Injections Due to Sterility Concerns
Promise Pharmacy, LLC is recalling 59 vials of IGF-1-LR3, 3 mg injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Product
IGF-1-LR3, 3 mg injection, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0434-2019·2019-02-20
Promise Pharmacy Recalls Prednisolone and Gatifloxacin Ophthalmic Solution for Sterility Concerns
Promise Pharmacy is recalling compounded Prednisolone and Gatifloxacin ophthalmic solution due to a lack of sterility assurance.
Product
Prednisolone and Gatifloxacin and Ketorolac Ophthalmic Solution 1%/0.5%/0.5%, Combo Drops: 3 mL Rx Only, Compounded Prescription, Promise Pharmacy 31818 US Hwy 19N, Palm Harbor FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0485-2019·2019-02-20
Dr. Reddy's Recalls Levetiracetam Injection Due to Labeling Error
Dr. Reddy's Laboratories is recalling Levetiracetam Injection bags because the primary label incorrectly identifies the product strength and sodium chloride concentration.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM INJECTION)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0433-2019·2019-02-20
Promise Pharmacy Recalls Prednisolone and Gatifloxacin Eye Drops for Sterility Concerns
Promise Pharmacy is recalling 55 bottles of compounded Prednisolone and Gatifloxacin Ophthalmic Solution due to a lack of sterility assurance.
Product
Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5%, Combo Drops 3 mL, Rx Only, Compounded Prescription, Promise Pharmacy 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0495-2019·2019-02-20
Tris Pharma Recalls Superpotent Infants' Ibuprofen Suspension
Tris Pharma is recalling 35,280 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 1 FL OZ (30 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39961 3, NDC 50428-1252-4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0493-2019·2019-02-20
Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration
Tris Pharma is recalling specific lots of Infants' Ibuprofen because the medication may contain a higher concentration of ibuprofen than labeled.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39338 3, NDC 59779-925-23.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0472-2019·2019-02-20
Promise Pharmacy Recalls Folic Acid Injection Due to Sterility Concerns
Promise Pharmacy, LLC is recalling Folic Acid Injection, 10 mg/mL, 10mL vials due to a lack of sterility assurance. The affected lots were distributed nationwide.
Product
Folic Acid, Injection, 10 mg/mL, 10mL vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0824-2019·2019-02-20
Steris ATLAS Loading Car Recalled for Latch Failure Risk
Steris Corporation is recalling 129 ATLAS Loading Cars because the latch may fail to engage when empty, causing the unit to slide or fall.
Product
ATLAS Loading Car
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0456-2019·2019-02-20
Promise Pharmacy Recalls IGF-1 LR3 Injections Due to Sterility Concerns
Promise Pharmacy is recalling 59 vials of IGF-1 LR3 injections because they lack sterility assurance. The affected products were distributed nationwide.
Product
IGF-1 LR3, 620 mcg injection, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0612-2019·2019-02-20
Philips CombiDiagnost R90 X-ray System Recalled for Radiation Dose Risk
Philips is recalling 146 CombiDiagnost R90 X-ray systems because a software defect may cause patients to receive increased radiation doses.
Product
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V112000·2019-02-20
Porsche Recalls One 2019 Cayenne Turbo for Shock Absorber Defect
Porsche is recalling one 2019 Cayenne Turbo because shock absorber forks may allow the shock absorbers to loosen, potentially impairing steering.
Product
PORSCHE — PORSCHE CAYENNE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0475-2019·2019-02-20
Promise Pharmacy Recalls Pyridoxine HCl Injection Due to Sterility Concerns
Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Product
Pyridoxine HCl, 100 mg/mL Injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
HighCPSC·19068·2019-02-20
Crate and Barrel Recalls Holiday Bear Acrylic Milk Bottles Due to Laceration Hazard
Crate and Barrel is recalling Holiday Bear Acrylic Milk Bottles because the included plastic straw can crack or break, posing a laceration hazard.
Product
Crate and Barrel Holiday Bear Acrylic Milk Bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V115000·2019-02-20
Porsche Recalls 14,110 Vehicles for Missing Brake Pad Warning
Porsche is recalling 14,110 vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out, increasing crash risk.
Product
PORSCHE — PORSCHE PANAMERA, PANAMERA 4 HYBRID EXECUTI, PANAMERA TURBO S HYBRID S, PANAMERA 4 HYBRID SPORT T
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V110000·2019-02-20
Volkswagen Recalls 2019 Jetta Vehicles for Incorrect Driver Airbag
Volkswagen is recalling 2019 Jetta vehicles because an incorrect driver frontal airbag may have been installed during a service visit, potentially increasing injury risk in a crash.
Product
VOLKSWAGEN — VOLKSWAGEN JETTA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0825-2019·2019-02-20
Hemotherm CE Dual Reservoir Cooler/Heater Recalled for Overheating Risk
Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.
Product
Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir Cooler/Heater is used to lower, maintain, or raise the temperature of the water flowing through a Blood Oxygenator / Heat Exchanger that is used to cool or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0834-2019·2019-02-20
Signature Orthopedics Recalls Three Genius Knee Cemented CR Femoral Components
Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.
Product
Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement component
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0823-2019·2019-02-20
Philips Ingenuity TF PET/CT Software Update Corrects Multiple Issues
Philips is issuing a software update for 24 Ingenuity TF PET/CT systems to correct multiple issues identified in the previous software version.
Product
Ingenuity TF PET/CT (non-RoHS), Model Number 882456 This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer reconstruction…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0826-2019·2019-02-20
Ottobock PushValve Recall for Diameter Specification Defect
Ottobock is recalling 538 PushValve units because some valve inserts have a diameter smaller than the specification. The valve is used for prosthetic fitting of lower limb amputees.
Product
21Y14 PushValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0489-2019·2019-02-20
Valeant Recalls Cardizem CD Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 390 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Product
CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0833-2019·2019-02-20
Signature Orthopedics Recalls Genius Knee Cemented Tibial Components Due to Product Mix-Up
Signature Orthopedics is recalling 10 Genius Knee Cemented Tibial Components due to a product mix-up. The recall covers units distributed in Florida, New York, and Tennessee.
Product
Genius Knee Cemented Tibial Component Product Usage: Knee replacement component
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0482-2019·2019-02-20
US Compounding Recalls LET Gel 4% Syringes Due to Missing Lot and Expiration Dates
US Compounding Inc is recalling 1,931 syringes of LET Gel 4% because the labels are missing specific lot and expiration dates.
Product
LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2019·2019-02-20
Valeant Recalls Cardizem CD Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 22 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Product
CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0828-2019·2019-02-20
Ottobock MagValve Recall for Prosthetic Socket Air Evacuation Defect
Ottobock is recalling 110 MagValve units used in prosthetic sockets because some valve inserts have a smaller diameter than specified.
Product
21Y15 MagValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
Category
Medical Device
Distribution
Distributed nationwide