State

New Jersey product recalls

73,738 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,780
Critical: 1,246
Severe: 2,942
Most recent: 2026-10-28

Of the 9,780 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 2,942 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32851–32875 of 83518

HighFDA (Devices)·Z-2051-2020·2020-05-27
Cardinal Health Recalls Strep B Carrot Broth Due to Temperature Abuse
Cardinal Health is recalling Strep B Carrot Broth One-Step tubes because they were stored outside approved temperature ranges, which may lead to patient misdiagnosis.
Product
Strep B Carrot Broth One-Step, 16x100mm Tube, 6ml, Item code Z46BX - Product Usage: Intended to detect Group B Streptococcus (GBS) from anovaginal specimen collected from pregnant women. If pregnant woman is positive for GBS colonization, this will indicate a need for treatment…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V308000·2020-05-27
Thor Motor Coach Recalls 2020 Motorhomes Due to Manual Error
Thor Motor Coach is recalling 566 2020 motorhomes because the owner's manual incorrectly describes the automatic parking function, which could lead to vehicle rollaway.
Product
THOR MOTOR COACH — THOR MOTOR COACH, THOR SIESTA, SYNERGY, GEMINI, DELANO
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2098-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Hemispherical Shells because the device may fall off its post in the inner packaging, resulting in loose coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 68 left, Sterile, Catalog # 504-02-68F-L, UDI (01)07613327012521(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2088-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled for Packaging Defect
Howmedica Osteonics is recalling Stryker Restoration Anatomic Hemispherical Shells because the device may fall off its post within the inner packaging, resulting in loose coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 56 Right, Sterile, Catalog # 504-02-56D-R, UDI (01)07613327012347(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2096-2020·2020-05-27
Stryker Restoration Anatomic Shell Recall Due to Packaging Defect
Howmedica Osteonics is recalling Stryker Restoration Anatomic Shells because the device may fall off its post in the inner packaging, resulting in coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 64 right, Sterile, Catalog # 504-02-64E-R, UDI (01)07613327012460(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2093-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled for Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shells because the device may detach from its post within the inner packaging, resulting in loose components and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 62 right, Sterile, Catalog # 504-02-62E-R, UDI (01)07613327012439(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2097-2020·2020-05-27
Stryker Restoration Anatomic Shell Recall Due to Packaging Defect
Howmedica Osteonics is recalling Stryker Restoration Anatomic Shells because the device may fall off its post within the inner packaging, resulting in loose components and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 66 right, Sterile, Catalog # 504-02-66F-R, UDI (01)07613327012477(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2091-2020·2020-05-27
Stryker Restoration Anatomic Shell Recall Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Hemispherical Shells because the device may fall off its post within the inner packaging, resulting in coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 60 right, Sterile, Catalog # 504-02-60D-R, UDI (01)07613327012408(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Drugs)·D-1282-2020·2020-05-27
West-Ward Recalls Ethacrynic Acid Tablets for Impurity Failures
West-Ward Columbus Inc is recalling Ethacrynic Acid Tablets USP, 25 mg, because the product failed impurity and degradation specifications.
Product
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2086-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shells because the device may fall off its post in the inner packaging, resulting in loose coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 56 Left, Sterile, Catalog # 504-02-56D-L, UDI (01)07613327012361(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2099-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shell devices because they may fall off their post in packaging, resulting in loose devices with coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 68 right, Sterile, Catalog # 504-02-68F-R, UDI (01)07613327012514(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2094-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics is recalling Stryker Restoration Anatomic Shells because the device may fall off its post within the inner packaging, resulting in loose components and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 64 left, Sterile, Catalog # 504-02-64E-L, UDI (01)07613327012484(17)
Category
Medical Device
Distribution
30 states
ModerateCPSC·20127·2020-05-27
Primark Recalls Kitten Heel Court Shoes Due to Chromium Levels
Primark is recalling Wide Fit Kitten Heel Court Pumps because the leather insoles contain elevated levels of Chromium VI, posing a risk of skin irritation.
Product
Wide Fit Kitten Heel Court Pumps
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2064-2020·2020-05-27
Philips HeartStart MRx Processor Board Replacement Kits Recalled for Damaged Bags
Philips is recalling HeartStart MRx Processor Board PCA Replacement Kits because damaged ESD bags were used for storing components.
Product
HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx Monitorl/Defibrillator - Product Usage: is intended for use in hospital and prehospital settings by qualified medical personnel trained in the operation of the device and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2045-2020·2020-05-27
Boston Scientific Recalls AMS 700 Reservoirs Due to Labeling Error
Boston Scientific is recalling five AMS 700 100 mL Spherical Reservoirs with InhibiZone because they were incorrectly labeled as a different model.
Product
AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the treatment of chronic, organic, male erectile dysfunction (impotence).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2067-2020·2020-05-27
DFINE Vertebral Hydraulic Assemblies Recalled for Incorrect Expiration Dates
Merit Medical Systems is recalling 228 DFINE Vertebral Hydraulic Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 1402 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological fractures…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2092-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shell devices because they may fall off their posts within the inner packaging, resulting in loose devices and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 62 left, Sterile, Catalog # 504-02-62E-L, UDI (01)07613327012453(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2073-2020·2020-05-27
Capso Vision Recalls CapsoCam Plus Capsule Endoscopy Systems Due to Labeling Errors
Capso Vision, Inc. is recalling 44 CapsoCam Plus video capsule systems because incorrect serial number labels may lead to patient misdiagnosis.
Product
CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2020·2020-05-27
Merit Medical Recalls DFINE Vertebral Assemblies Due to Incorrect Expiration Dates
Merit Medical Systems is recalling 63 DFINE Vertebral Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 3427 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1271-2020·2020-05-27
Mylan Recalls Aloprim Injection Vials Due to Discoloration
Mylan Institutional LLC is recalling 3,010 vials of Aloprim (allopurinol sodium) for Injection due to out-of-specification appearance and color results.
Product
ALOPRIM — ALOPRIM (ALLOPURINOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2089-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Hemispherical Shells because the device may fall off its post within the inner packaging, resulting in loose components and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 58 Right, Sterile, Catalog # 504-02-58D-R, UDI (01)07613327012446(17)
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2085-2020·2020-05-27
Stryker Restoration Anatomic Shell Recalled for Packaging Defect
Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shell devices because they may fall off their post within the inner packaging, resulting in loose devices and coating debris.
Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Right, Sterile, Catalog # 504-02-54C-R, UDI (01)07613327012415(17)
Category
Medical Device
Distribution
30 states
LowFDA (Drugs)·D-1272-2020·2020-05-27
InvaGen Recalls Gabapentin Tablets Due to Impurity Test Failure
InvaGen Pharmaceuticals is recalling 2,202 bottles of Gabapentin 600 mg tablets because they failed an impurity test during stability testing.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2038-2020·2020-05-27
Pega Medical Recalls SLIM System Handle Due to Lot Number Mismatch
Pega Medical Inc. is recalling three units of the SLIM System handle because the lot number on the instrument does not match the packaging label.
Product
Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V301000·2020-05-26
Altec Recalls Aerial Devices With Incorrect Tow Hitch Load Ratings
Altec is recalling 2014-2020 Aerial Devices with Class 3 towing hitches that may have incorrect load ratings or damage from overloading, increasing crash risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide