State

Northern Mariana Islands product recalls

72,971 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 22
Critical: 0
Severe: 8
Most recent: 2025-02-05

Of the 22 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 8 (36%) are Severe.

Which agencies issued them

These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5951–5975 of 72993

HighFDA (Drugs)·D-0501-2025·2025-07-09
Compounded ketamine multi-dose vials recalled over sterility assurance concerns
Ketamine Hydrochloride Injection 500 mg/5 mL multi-dose vials compounded by Medivant Healthcare are being recalled for lack of assurance of sterility. 14,725 vials are affected.
Product
KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0007-2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2054-2025·2025-07-09
Philips L12-3 ultrasound transducers were refurbished beyond their useful life
Philips L12-3 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips L12-3 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2067-2025·2025-07-09
Philips X8-2t ultrasound transducers were refurbished beyond their useful life
Philips X8-2t Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips X8-2t Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2059-2025·2025-07-09
Philips S7-2 Transducer Ultrasound Devices Recalled for Refurbishment
Philips Ultrasound, Inc. is recalling Philips S7-2 Transducer ultrasound devices that were refurbished beyond their useful life. The affected devices have been distributed domestically and internationally.
Product
Philips S7-2 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2055-2025·2025-07-09
Philips L12-4 Ultrasound Transducers Refurbished Beyond Useful Life
Philips Ultrasound, Inc. is recalling 5,230 Philips L12-4 ultrasound transducer devices that were refurbished beyond their useful life. Affected units were distributed domestically and to numerous countries worldwide.
Product
Philips L12-4 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2060-2025·2025-07-09
Philips S7-3t ultrasound transducers were refurbished beyond their useful life
Philips S7-3t Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips S7-3t Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2025·2025-07-09
Philips XL14-3 Ultrasound Transducer Refurbished Beyond Useful Life
Philips Ultrasound, Inc. is recalling Philips XL14-3 Transducers because they were refurbished beyond their useful life, which may affect device performance and patient safety during ultrasound examinations.
Product
Philips XL14-3 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0507-2025·2025-07-09
Gabapentin Capsules 100 mg recalled for defective blister packaging
The Harvard Drug Group LLC is recalling 23,232 cartons of Gabapentin Capsules 100 mg (Lot# M05205, Exp Date 10/2026) distributed nationwide due to inadequately sealed blister packaging that may compromise product integrity.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2086-2025·2025-07-09
ADVIA hematology calibrator lots carry incorrect platelet value assignments
ADVIA 120/2120/2120i SETpoint Calibrator lots are being recalled because they have the incorrect platelet value assignments for ADVIA hematology systems. 2,020 units are affected.
Product
ADVIA¿ 120/2120/2120i SETpoint Calibrator
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0508-2025·2025-07-09
Gabapentin capsule bags recalled because blister packaging was inadequately sealed
Gabapentin Capsules 100 mg from Major Pharmaceuticals are being recalled because of a defective container: the blister packaging was inadequately sealed. 3,527 bags are affected.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2038-2025·2025-07-09
VITROS 5600 Integrated System software anomaly reported
Ortho-Clinical Diagnostics is recalling the VITROS 5600 Integrated System due to a software anomaly that can report test results using expired reagents even when the use-expired-reagents setting is disabled, potentially causing erroneous or delayed test results.
Product
Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog Number: (1) 6802413, (2) 6802915
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2049-2025·2025-07-09
Philips C5-1 ultrasound transducers were refurbished beyond their useful life
Philips C5-1 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips C5-1 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2057-2025·2025-07-09
Philips L9-3 ultrasound transducers were refurbished beyond their useful life
Philips L9-3 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips L9-3 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2064-2025·2025-07-09
Philips X5-1 ultrasound transducers were refurbished beyond their useful life
Philips X5-1 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips X5-1 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2075-2025·2025-07-09
BD Heyman Coude Tip Catheters Recalled Over French Size Labeling Error
C.R. Bard Inc is recalling certain BD Heyman Follower Coude Tip catheters because the packaging may display the incorrect French size, which could lead to use of the wrong size device.
Product
BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2052-2025·2025-07-09
Philips eL18-4 Ultrasound Transducers Recalled for Defective Refurbishment
Philips Ultrasound is recalling Philips eL18-4 Transducers because they were refurbished beyond their useful life, which may affect device performance and patient safety.
Product
Philips eL18-4 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2056-2025·2025-07-09
Philips L8-4 Ultrasound Transducers Recalled for Refurbishment Beyond Useful Life
Philips Ultrasound is recalling 5,230 L8-4 transducer units that were refurbished beyond their useful life, which may affect device safety and performance. The units were distributed nationwide and internationally.
Product
Philips L8-4 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2073-2025·2025-07-09
VITROS opiate reagent lots may give low quality control results
VITROS Chemistry Products OP Reagent Gen 15 lots are being recalled because they may generate lower than expected quality control results. 2,017 units are affected.
Product
VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 1997. The VITROS OP Reagent is a dual-chambered package containing ready-to-use liquid reagents that are used to detect opiates in urine. One sales unit contains 6 Microtip packs of reagent. Each pack has 50 OP tests.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2066-2025·2025-07-09
Philips X7-2t ultrasound transducers were refurbished beyond their useful life
Philips X7-2t Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips X7-2t Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2088-2025·2025-07-09
ADVIA Hematology Control Recalled for Incorrect Platelet Value Assignments
Siemens Healthcare Diagnostics is recalling ADVIA 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) units because they have incorrect platelet value assignments for the hematology systems.
Product
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2050-2025·2025-07-09
Philips C5-2 Ultrasound Transducers Refurbished Beyond Useful Life
Philips Ultrasound, Inc. is recalling Philips C5-2 Transducers because they were refurbished beyond their useful life. The affected devices were distributed domestically nationwide and internationally across 49 countries.
Product
Philips C5-2 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2063-2025·2025-07-09
Philips VL13-5 ultrasound transducers were refurbished beyond their useful life
Philips VL13-5 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
Product
Philips VL13-5 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2070-2025·2025-07-09
HemoCue glucose microcuvettes experienced transit time outside of specified limits
Four boxes of HemoCue Glucose 201 Microcuvettes are being recalled because transit time fell outside limits, so stability through the microcuvette lifetime can no longer be guaranteed.
Product
The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 (or DM) Analyzer with plasma conversion that multiplies the measured whole blood glucose value by a factor of 1.112 and displays a plasma equivalent glucose result. HemoCue Glucose 201 Microcu
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2077-2025·2025-07-09
ColoSense Test Kit Components Recalled for Control Failures
Geneoscopy, Inc. is recalling ColoSense Test Kit Part No. 80-001 (Lot 80-001-A2501) due to multiple plate failures caused by Low Positive Template Control being too high and out of range.
Product
ColoSense Test Kit, Part No. 80-001, component of ColoSense test
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2087-2025·2025-07-09
ADVIA hematology control lots carry incorrect platelet value assignments
ADVIA 120/2120/2120i 3-in-1 TESTpoint Control lots are being recalled because they have the incorrect platelet value assignments for ADVIA hematology systems. 4,214 units affected.
Product
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control)
Category
Medical Device
Distribution
Distributed nationwide