State

New Jersey product recalls

73,809 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,782
Critical: 1,246
Severe: 2,944
Most recent: 2026-11-04

Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38726–38750 of 83591

SevereFDA (Drugs)·D-1267-2019·2019-05-08
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, 50mg/12.5mg, a) 30-count (NDC: 13668-116-30), b) 90-count (NDC: 13668-116-90), c) 1000-count (NDC: 13668-116-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1256-2019·2019-05-08
Customceutical Compounding Recalls HCG Injection Vials Due to Sterility Concerns
Customceutical Compounding is recalling 12 vials of compounded HCG injection due to a lack of assurance of sterility. The product was distributed nationwide.
Product
HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 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-1253-2019·2019-05-08
Customceutical Compounding Recalls BPlex Injectable Vials Due to Sterility Concerns
Customceutical Compounding is recalling 32 vials of BPlex injectable compound because the product lacks assurance of sterility. The recall covers products distributed nationwide.
Product
BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV 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-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 (Food)·F-1318-2019·2019-05-08
Harmless Harvest Recalls Strawberry Coconut Drink Due to Packaging Defect
Harmless Harvest is voluntarily recalling specific lots of its Strawberry Probiotic Coconut Drink due to a packaging defect that may cause premature spoilage.
Product
Harmless Harvest Dairy-Free Yogurt Drink; Cultured Coconut Drink - Probiotic Strawberry. 8 fl. oz. plastic bottle; UPC 859078-002979
Category
Food
Distribution
4 states
ModerateFDA (Food)·F-1317-2019·2019-05-08
Harmless Harvest Recalls Dairy-Free Yogurt Drink Due to Packaging Defect
Harmless Harvest Inc. is voluntarily recalling specific lots of its Dairy-Free Yogurt Drink due to a packaging defect that may cause premature spoilage.
Product
Harmless Harvest Dairy-Free Yogurt Drink; Cultured Coconut Drink; Probiotic Original Unsweetened. 8 fl. oz. plastic bottle; UPC 859078-002962 USDA Organic
Category
Food
Distribution
4 states
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 (Food)·F-1321-2019·2019-05-08
Lamb Weston Recalls Potato Tater Puffs Due to Plastic Contamination
Lamb Weston BSW LLC is recalling specific lots of Lamb's Supreme Potato Tater Puffs due to potential contamination with plastic objects.
Product
Lamb s Supreme Potato Tater Puffs, item # H30, packaged in 5-pound unprinted KRAFT paper bags, 6 bags to a case, sold as a foodservice item. UPC 1 00 44979 00830 5. The case label is read in parts: "***LAMB'S SUPREME TATER PUFFS***FROZEN POTATOES***6/5 LB BAGS***Produced by…
Category
Food
Distribution
19 states
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