State

New Jersey product recalls

72,820 recalls have nationwide distribution and so reach New Jersey. 9,751 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,751
Critical: 1,249
Severe: 2,480
Most recent: 2026-09-09

Of the 9,751 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,480 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,751 recalls whose distribution notice names New Jersey specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

751–775 of 82571

SevereFDA (Drugs)·D-0672-2026·2026-07-15
Pemetrexed for Injection recalled due to lack of sterility assurance
Reliance Life Sciences is recalling Pemetrexed for Injection 500mg/Vial nationwide due to lack of sterility assurance. The affected product may not meet required sterility standards for intravenous use.
Product
Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2710-2026·2026-07-15
Fletcher CT/MR Shielded Applicator Set for Gynecological Brachytherapy Recalled
Elekta's Fletcher CT/MR Shielded Applicator Set is recalled due to risk that the tip of the intrauterine tube may detach and remain inside a patient during gynecological brachytherapy treatment.
Product
Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2712-2026·2026-07-15
Elekta Geneva Brachytherapy Applicator Intrauterine Tube Detachment Risk
Elekta is recalling the Geneva Brachytherapy Applicator due to a safety concern that the tip of the intrauterine tube may detach and remain inside a patient during cancer treatment.
Product
Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0671-2026·2026-07-15
Pemetrexed for Injection Recalled Due to Lack of Sterility Assurance
Somerset Therapeutics is recalling Pemetrexed for Injection 100mg/Vial due to lack of sterility assurance. The recall affects approximately 12,000 vials distributed nationwide.
Product
Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2711-2026·2026-07-15
Brachytherapy Applicator Advanced Gynecological Applicator Tip Detachment
Elekta, Inc. is recalling Advanced Gynecological Applicators due to potential detachment of the intrauterine tube tip, which may remain inside a patient during cancer treatment.
Product
Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2716-2026·2026-07-15
TMINI Tracking Array knob loosening causing potential array misalignment
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays used in knee replacement surgery because the knob on the tracking array may loosen, causing potential misalignment of the array.
Product
TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0673-2026·2026-07-15
Bortezomib for Injection Recalled Due to Lack of Sterility Assurance
Bortezomib for Injection 3.5mg/Vial manufactured by Reliance Life Sciences is being recalled nationwide due to lack of sterility assurance. Affected lots include RBIH0125A, RBIH0225A, RBIH0325A, and RBIH0525A distributed across the USA.
Product
Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0674-2026·2026-07-15
Azacitidine for Injection Recalled for Lack of Sterility Assurance
Reliance Life Sciences is recalling Azacitidine for Injection 100mg/Vial nationwide due to lack of sterility assurance. Patients using affected lots should contact their healthcare provider.
Product
Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Intravenous Use, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0857-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1150-2026·2026-07-15
High Valley Orchard Chocolate Covered Raisins Recalled for Undeclared Peanut
High Valley Orchard Chocolate Covered Raisins (15oz bags) are recalled nationwide due to undeclared peanut from mis-packaging. Consumers with peanut allergies should not consume this product.
Product
High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is packaged in clear plastic container. UPC on retail container: 0 952348 80170 0. The label of affected product declares: INGREDIENTS: MILK CHOCOLATE (SUGAR,
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2694-2026·2026-07-15
Intracept Access Instruments sterile barrier breach risk
Boston Scientific is recalling Intracept Access Instruments due to potential sterile barrier breach in the outer tray seal, which could introduce infection risk.
Product
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2703-2026·2026-07-15
Atellica CH Enzymatic Hemoglobin A1c assay well-to-well bias
Siemens is recalling an A1c blood test assay (Material Number 11097536) for the Atellica CH and Atellica CI analyzers due to potential intermittent bias that could cause falsely high or low hemoglobin A1c patient results.
Product
Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0670-2026·2026-07-15
Drogueria San Juan Isopropyl Alcohol 70% recalled for subpotency
Gasco Industrial Corp. is recalling Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% (32 oz.) due to subpotency. Affected lots 250206B1, 250218B2, and 250507B1 were distributed nationwide in the US.
Product
Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana Llana Rio Piedras, PR 00924, UPC 659685696567.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2677-2026·2026-07-15
Aquacel Ag Surgical SP Surgical Dressing Recalled for Out-of-Specification Thickness
ConvaTec is recalling Aquacel Ag Surgical SP dressings (Lot 5G00809) that were manufactured with greater-than-specified thickness. The dressing is used in surgical wound care.
Product
Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2714-2026·2026-07-15
OmniTract Surgical Retractor System sterilization instructions require extended dry time
Integra LifeSciences is recalling the OmniTract Surgical Retractor System because the sterilization instructions require a longer dry time than stated in the current manual. The dry time must be extended to 90, 110, or 120 minutes depending on the sterilization cycle used.
Product
OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0666-2026·2026-07-15
Gasco Isopropyl Alcohol 70% recalled nationwide for subpotency
Gasco Industrial Corp. is recalling Gasco Isopropyl Alcohol 70% (1 US Gallon) nationwide due to subpotency. The voluntary recall affects specific lot numbers manufactured before the expiration date.
Product
Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial Corp., PO Box 1360, Gurabo, PR 00778, Made in USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2702-2026·2026-07-15
5008X Blood Tubing Set connection errors FDA Class II recall
Fresenius Medical Care is recalling 5008X Blood Tubing Sets due to potential online port errors that may occur when connecting the SafeLine to the substitution fluid port of the 5008X CAREsystem.
Product
5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF St
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2695-2026·2026-07-15
Medline Anesthesia Kit Peds Contains Defective Temperature Probes
Medline Industries is recalling Anesthesia Kit Peds (Model DYNJAP10125A, Lot 24JBR072) nationwide because they contain Covidien Mon-a-Therm temperature probes affected by a distribution control error.
Product
Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2676-2026·2026-07-15
Olympus Single Use Distal Cover MAJ-2315 Duodenovideoscope Replacement
Olympus Corporation of the Americas is replacing the previous design of its Single Use Distal Cover (MAJ-2315) with a newly designed version for use with EVIS EXERA III Duodenovideoscopes.
Product
Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flex
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1146-2026·2026-07-15
Wise Onion Rings recalled for undeclared food color additives
Wise Foods Inc is recalling Wise Onion Rings, 3.75 oz packages, because they contain undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3 food colorings that are not listed on the label.
Product
Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0663-2026·2026-07-15
Medline Remedy Specialized Silicone Cream Recalled for Elevated Formaldehyde Levels
Medline Remedy Specialized Silicone Cream is being recalled because formaldehyde levels exceeded the product specification. BioMed Laboratories is recalling approximately 509,652 tubes distributed nationwide.
Product
MEDLINE — MEDLINE (DIMETHICONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0662-2026·2026-07-15
Methohexital Sodium for Injection Recalled for Failed Impurities and Degradation Specifications
OneSource Specialty Pharma Limited is recalling one lot of Methohexital Sodium for Injection due to failed impurities and degradation specifications. The affected product was distributed nationwide.
Product
METHOHEXITAL SODIUM — METHOHEXITAL SODIUM (METHOHEXITAL SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateNHTSA·26V455000·2026-07-15
2022 Nissan Armada and Infiniti QX vehicles with incorrect GAWR label
Nissan is recalling certain 2020–2026 Nissan Armada and 2011–2027 Infiniti QX56/QX80 vehicles with 22" wheels because the Gross Axle Weight Rating on the certification label is incorrect, which can allow the vehicle to be overloaded and increase crash risk.
Product
INFINITI — INFINITI, NISSAN QX80, ARMADA, QX56
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2697-2026·2026-07-15
Medline Open Heart Peds Pack Convenience Kits Temperature Probe Recall
Medline Industries is recalling specific lots of Open Heart Peds Pack Convenience Kits containing Covidien Mon-a-Therm temperature probes due to a distribution control process error.
Product
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2717-2026·2026-07-15
Versius Surgical System Console affected by cybersecurity vulnerability
CMR Surgical Limited is recalling the Versius Surgeon Console (Model V-SS-1020, Software Version Pratchett 1 version 62.1) due to Secure Boot not being enabled at manufacturing, presenting a potential cybersecurity risk.
Product
Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0667-2026·2026-07-15
Gasco Isopropyl Alcohol 70% recalled for subpotent drug content
Gasco Industrial Corp. is recalling Gasco Isopropyl Alcohol 70% (32 oz bottles, Lot 250218B3) distributed nationwide because the product is subpotent—containing less active ingredient than labeled.
Product
Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UPC 7 87302 12363 6.
Category
Drug
Distribution
Distributed nationwide