State

New Jersey product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44176–44200 of 83606

SevereFDA (Devices)·Z-1603-2018·2018-05-09
Philips MultiDim Eleva Imaging System Recalled for Uncontrolled Table Rotation
Philips is recalling 184 MultiDim Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Product
MultiDim Eleva 708032 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1605-2018·2018-05-09
Philips MultiDiagnost Eleva Imaging System Recalled for Uncontrolled Table Rotation
Philips is recalling 37 MultiDiagnost Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Product
MultiDiagnost Eleva 708036 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0706-2018·2018-05-09
AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns
AuroMedics Pharma LLC is recalling Levetiracetam Injection due to a lack of assurance of sterility and a confirmed report of leaking bags and mold.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1174-2018·2018-05-09
Ignite Pre-Workout Supplement Recalled for Undeclared Milk Allergen
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement because the label declares whey protein but fails to declare milk.
Product
Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2. Ignite High Endurance Pre-Workout Supplement with CAFFEINE, brand Muscle Sports & Nutrition (MSN), Net wt. 1 lb. UPC 8 01650 01540 2 and UPC 8 01650 01541 9.
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1607-2018·2018-05-09
Philips MD-Eleva Medical Imaging System Recalled for Tilt Actuator Failure
Philips is recalling 199 MD-Eleva imaging systems because a tilt actuator may break, causing the table to rotate uncontrollably at high speed.
Product
Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1606-2018·2018-05-09
Philips MD-Eleva Imaging System Recalled for Uncontrolled Table Rotation
Philips is recalling 206 MD-Eleva imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Product
Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1538-2018·2018-05-09
Zimmer Biomet Recalls Modular Hip Head Components Due to Sizing Errors
Zimmer Biomet is recalling 18 modular hip head components because two lots of different sizes were potentially commingled. This may lead to the use of an incorrect sized head.
Product
Modular Head Component, Biomet Hip System; Item No. 11-363661, Hip Joint, metal/polymer/metal, semi-constrained, porous-coated, uncemented prosthesis The device is used in treatment of patients who need total hip arthroplasty, and consists of modular components and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0804-2018·2018-05-09
Sanofi Recalls Over-Concentrated Docetaxel Injection Vials Nationwide
Sanofi-Aventis is recalling 19,580 vials of Docetaxel injection concentrate due to potential over-concentration. The affected lots were distributed nationwide.
Product
DOCETAXEL — DOCETAXEL (DOCETAXEL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0704-2018·2018-05-09
AuroMedics Recalls Levofloxacin IV Bags Due to Sterility Concerns
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0707-2018·2018-05-09
AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns
AuroMedics Pharma LLC is recalling 67,300 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1609-2018·2018-05-09
Philips MultiDiagnostic-Eleva Imaging System Recalled Due to Uncontrolled Table Rotation
Philips is recalling the MultiDiagnostic-Eleva imaging system because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Product
MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0708-2018·2018-05-09
AuroMedics Recalls Levofloxacin Injection Bags Due to Sterility Concerns
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and reports of leaking bags with mold.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1178-2018·2018-05-09
Clean Athletics Enduravol Elite Pre-Workout Recalled for Undeclared Milk Allergen
Independent Nutrition, Inc. is recalling Enduravol Elite Pre-Workout because the label declared whey protein but failed to declare milk, a major allergen.
Product
Enduravol Elite Pre-Workout, brand Clean Athletics. Net wt. 1 lbs. No UPC.
Category
Food
Distribution
6 states
SevereFDA (Food)·F-1176-2018·2018-05-09
Ignite Pre-Workout Supplement Recalled for Undeclared Milk Allergen
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement because the label declared whey protein but failed to declare milk.
Product
Ignite High Endurance Pre-Workout Supplement, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01541 9. Ignite High Endurance Pre-Workout Supplement, brand Healthy Home Center Inc., Net wt. 1 lb. UPC 8 01650 01541 9. Ignite High Endurance Pre-Workout Supplement, brand…
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1608-2018·2018-05-09
Philips MultiDiagnostic-Eleva Recalled Due to Uncontrolled Table Rotation Hazard
Philips Medical Systems is recalling 184 MultiDiagnostic-Eleva systems because a broken actuator fixation can cause the table to rotate uncontrollably at high speed.
Product
MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1604-2018·2018-05-09
Philips URODiagnost Imaging System Recalled Due to Uncontrolled Table Rotation
Philips Medical Systems is recalling 20 URODiagnost imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Product
708033 URODiagnost As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1476-2018·2018-05-09
FDA Recalls Mitragyna Speciosa Leaf Powder Due to Salmonella Contamination Risk
Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder products because they may be contaminated with Salmonella.
Product
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Exhaust Lines Due to Sterility Concerns
Cook Inc. is recalling 760 StoneBreaker Exhaust Lines because the interior may not be properly sterilized during reprocessing.
Product
StoneBreaker Exhaust Line, Catalog number: SBA-EL; GPN: G52600; UDI: (01)00827002526006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1144-2018·2018-05-09
Purely Elizabeth Granola Recalled for Undeclared Soy Lecithin
Purely Elizabeth is recalling Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin. The product was distributed nationwide.
Product
Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1540-2018·2018-05-09
Siemens Dimension Vista Calcium Flex Reagent Cartridge Recalled for Low Results
Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium Flex reagent cartridges because they may produce erroneously low results from specific well sets.
Product
Dimension Vista¿ Calcium Flex¿ reagent cartridge, Dimension Vista¿ CA, K1023, SMN # 10445160 The CA method is an in vitro diagnostic test for the quantitative measurement of calcium in human serum, plasma, and urine on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2018·2018-05-09
Cook Inc. Recalls StoneBreaker C02 Cartridges Due to Sterility Concerns
Cook Inc. is recalling 38,542 StoneBreaker C02 Cartridges because the interior may not be sterilized to the appropriate level when reprocessed.
Product
StoneBreaker C02 Cartridge, Catalog number: SBC-10; GPN: G52603; UDI: (01)10827002526034
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Probe Caps Due to Sterility Concerns
Cook Inc. is recalling 370 StoneBreaker Probe Caps because the interior may not be properly sterilized during reprocessing.
Product
StoneBreaker Probe Cap, Catalog number:SBA-PC; GPN: G52601; UDI:(01)00827002526013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1591-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Exhaust Caps Due to Sterility Concerns
Cook Inc. is recalling 629 StoneBreaker Exhaust Caps because the interior may not be sterilized to the appropriate level when following reprocessing instructions.
Product
StoneBreaker Exhaust Cap, Catalog number: SBA-EC; GPN: G52599; UDI: (01)00827002525993
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18740·2018-05-09
Wrapables Recalls Women's Silk Scarves for Flammability Standard Violation
Wrapables is recalling about 1,900 women's silk scarves because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Women's scarves
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V302000·2018-05-09
Triumph Recalls 2018 Street Triple Motorcycles for Switch Malfunction
Triumph is recalling 2018 Street Triple R and RS motorcycles because water intrusion can cause the turn signal and headlight switches to malfunction, increasing crash risk.
Product
TRIUMPH — TRIUMPH STREET TRIPLE S
Category
Vehicle
Distribution
Distributed nationwide