State

Northern Mariana Islands product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33951–33975 of 73757

SevereFDA (Drugs)·D-1260-2019·2019-05-08
Customceutical Compounding Recalls Test PROCYP Injectable Due to Sterility Concerns
Customceutical Compounding is recalling Test PROCYP injectable vials because the company cannot guarantee the product is sterile.
Product
Test PROCYP (TESTOSTERONE CYPIONATE 200MG/ML TESTOSTERONE PROPIONATE 20MG/ML), 5 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1269-2019·2019-05-08
Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.
Product
Losartan Potassium and Hydrochlorothiazide Tablets, USP, 100mg/25mg, a) 30-count (NDC: 13668-118-30) b) 90-count (NDC: 13668-118-90), c) 1000-count (NDC: 13668-118-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1255-2019·2019-05-08
Customceutical Compounding Recalls Glutathione Injection Vials Due to Sterility Concerns
Customceutical Compounding is recalling specific lots of compounded Glutathione 200mg/mL injection vials because the FDA could not ensure the products were sterile.
Product
Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML MULTIDOSE VIAL MDV Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1259-2019·2019-05-08
Customceutical Compounding Recalls Test D Vials Due to Sterility Concerns
Customceutical Compounding is recalling Test D vials because the manufacturer cannot ensure the injectable solution is sterile.
Product
Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1250-2019·2019-05-08
AvKARE Recalls Losartan Potassium Tablets Due to Impurity
AvKARE Inc. is recalling Losartan Potassium Tablets 25 mg because FDA testing found an impurity above acceptable levels.
Product
Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Dose Rx Only NDC 50268-516-15 Manufactured for: AvKARE Inc. Pulaski, TN 38478
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1226-2019·2019-05-08
DePuy Spine Recalls Concorde Lift Spinal Fusion Implants Due to Migration
DePuy Spine is recalling Concorde Lift spinal fusion implants because a complaint trend was observed for post-operative loss of height and migration.
Product
Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1265-2019·2019-05-08
Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity
Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found an impurity above acceptable levels.
Product
Losartan Potassium Tablets, USP, 50 mg, a) 90-count (NDC: 13668-409-90), b)1000-count (NDC: 13668-409-10) per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1247-2019·2019-05-08
Siemens CT Scanners Recalled for Dual Energy Scan Abortion Risk
Siemens is recalling 53 SOMATOM Definition AS CT scanners due to a software issue that may cause scans to abort when using the optional Dual Spiral Dual Energy mode.
Product
SOMATOM Definition AS with Option syngo DE Scan for Single Source (Dual Spiral Dual Energy scan mode), Model Number 8098027 Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1251-2019·2019-05-08
Advanced Pharma Recalls Sub-Potent Hydromorphone Injectable Solution
Advanced Pharma Inc. is voluntarily recalling 560 bags of compounded Hydromorphone 20 mg/100 mL Injectable Solution due to sub-potency. The product was distributed nationwide in the US.
Product
HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10
Category
Drug
Distribution
Distributed nationwide
HighCPSC·19117·2019-05-08
Igloo Recalls Marine Elite Coolers Due to Entrapment and Suffocation Hazards
Igloo is recalling Marine Elite coolers because the stainless-steel latch can automatically lock, posing entrapment and suffocation hazards to children.
Product
Igloo Marine Elite Coolers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1225-2019·2019-05-08
DePuy Spine Recalls Concorde Lift Spinal Fusion Implants
DePuy Spine is recalling Concorde Lift spinal fusion implants due to a complaint trend of post-operative loss of height and migration.
Product
Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (197811026C), 9x21 (US197809021C), 9x26 (US197809026C)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1244-2019·2019-05-08
Siemens CT Scanner Recall Due to Software Issue in Dual Spiral Mode
Siemens is recalling 53 SOMATOM Confidence CT scanners due to a software issue that may cause scans to abort when using the optional Dual Spiral Dual Energy mode.
Product
SOMATOM Confidence, Model Number 10590100 Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1238-2019·2019-05-08
PerkinElmer AutoDELFIA hCG Kit Recalled for Potential Measurement Inaccuracy
PerkinElmer is recalling AutoDELFIA hCG Kits because hCG concentrations may be decreased by 15-20% at the lower measuring range.
Product
AutoDELFIA¿ hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code: B007-101 - Product Usage: Quantitative determination of human gonadotrophin (hCG).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1243-2019·2019-05-08
Molnlycke Recalls EZ Derm Porcine Xenograft Due to Heat Seal Failures
Molnlycke Health Care is recalling 1,332 units of EZ Derm Porcine Xenograft due to intermittent heat seal failures on the outer pouch.
Product
EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03; b. EZ Derm 7 x 18 (17 x 46 cm) Non-Perforated, Part Number: 131704-03; c. EZ Derm 2 x 2 (5 x 5 cm) Non-Perforated, Part Number: 131705-03; d.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1242-2019·2019-05-08
BioFire FilmArray Gastrointestinal Panel Recalled for False Positive Results
BioFire Diagnostics is recalling the FilmArray Gastrointestinal (GI) Panel due to elevated rates of false positive results for Campylobacter and Cryptosporidium.
Product
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116), Product Usage: The FilmArray Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test intended for use with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1235-2019·2019-05-08
Siemens Atellica IM aTG Test Kits Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling 1,489 Atellica IM aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.
Product
Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN): 10995461
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1223-2019·2019-05-08
Matrix Surgical Recalls 46 OmniPore Implants Due to Mislabeling
Matrix Surgical Holdings is voluntarily recalling 46 OmniPore Surgical Implants due to product mislabeling. The recall covers units distributed in the US and several international countries.
Product
OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: OmniPore Surgical Implants in block, sheet, and anatomical shapes are intended for nonweight bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. OmniPore…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1236-2019·2019-05-08
Siemens Atellica IM aTG Test Kits Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling 114 Atellica IM aTG test kits because they show positive bias compared to WHO standards.
Product
Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1224-2019·2019-05-08
Matrix Surgical Recalls 42 OmniPore Implants Due to Mislabeling
Matrix Surgical Holdings is recalling 42 OmniPore Surgical Implants due to product mislabeling. The recall covers units distributed in the US and several international countries.
Product
OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: OmniPore Surgical Implants in block, sheet, and anatomical shapes are intended for nonweight bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. OmniPore…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1271-2019·2019-05-08
AmEx Pharmacy Recalls Bevacizumab Syringes Due to Defective Delivery System
AmEx Pharmacy is recalling 249 syringes of Bevacizumab intravitreal injection because the delivery system is difficult to express.
Product
BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This biologic product was repackaged by AmEx Pharmacy 1515 Elizabeth St. Suite J Melbourne, FL 32901 Lot:190212AB BUD:5/13/2019, Repackaged on 2/12/2019
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1246-2019·2019-05-08
Siemens CT Scanner Recall for Potential Scan Abortion in Dual Mode
Siemens is recalling 53 SOMATOM Edge Plus CT scanners due to a software issue that may cause scans to abort when using the optional Dual Spiral Dual Energy mode.
Product
SOMATOM Edge Plus, Model Number 10267000 Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1237-2019·2019-05-08
PerkinElmer Recalls DELFIA hCG Kits Due to Measurement Inaccuracy
PerkinElmer is recalling 31 DELFIA hCG Kits because hCG concentrations may be decreased by 15-20% at the lower measuring range.
Product
DELFIA¿ hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code: A007-101 - Product Usage: Quantitative determination of human gonadotrophin (hCG) in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1276-2019·2019-05-08
American Health Packaging Recalls Glipizide Extended-Release Tablets for Dissolution Failure
American Health Packaging is recalling 2,203 cartons of Glipizide Extended-Release Tablets, 2.5 mg, due to failed dissolution specifications at time zero.
Product
GlipiZIDE Extended-release Tablets, 2.5 mg, 30 Tablets (3 x 10), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC: 68084-295-21
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1233-2019·2019-05-08
Siemens ADVIA Centaur aTG Test Kits Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling ADVIA Centaur aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.
Product
Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number (SMN): 10492398
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1234-2019·2019-05-08
Siemens ADVIA Centaur aTG Test Kits Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling ADVIA Centaur aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.
Product
SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN): 10492399
Category
Medical Device
Distribution
Distributed nationwide