The Recall Desk

State

New Jersey product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29301–29325 of 83502

  • HighFDA (Devices)·Z-1173-2021·2021-03-10

    Siemens Sensis Vibe Systems Recalled for Potential System Freezes

    Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.

    Product
    Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0296-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system is out of specification for mechanical peel.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1153-2021·2021-03-10

    Bovie Velocity Disposable Bipolar Ablators Recalled for Sterile Packaging Defect

    Bovie Medical Corporation is recalling Velocity Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.

    Product
    Velocity Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1170-2021·2021-03-10

    Boston Scientific Recalls Polypectomy Snares Due to Incomplete Pouch Seals

    Boston Scientific is recalling Captivator, Captiflex, and Sensation polypectomy snares because users reported incomplete pouch seals before use.

    Product
    Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0293-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 473,280 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0295-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 786,900 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1155-2021·2021-03-10

    Bovie Medical Recalls ConMed Disposable Bipolar Ablators Due to Packaging Defect

    Bovie Medical Corporation is recalling 5,270 ConMed Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.

    Product
    ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0292-2021·2021-03-10

    Dr. Reddy's Recalls Progesterone Capsules Due to Dissolution Failures

    Dr. Reddy's Laboratories is recalling 16,449 bottles of 200 mg Progesterone Capsules because stability testing revealed out-of-specification dissolution results.

    Product
    PROGESTERONE — PROGESTERONE (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1164-2021·2021-03-10

    G & H Wire Company Recalls Orthodontic Elastic Bands Due to Labeling Error

    G & H Wire Company is recalling orthodontic elastic bands because the patient pack text is incorrect, which could lead to misuse and temporary discomfort.

    Product
    Band, Elastic, Orthodontic - Product Usage: Orthodontic elastics, also referred to as rubber bands, are small stretchy loops of rubber that help move teeth into proper alignment during orthodontic treatment. Their purpose is to create additional force for tooth movement in any…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1154-2021·2021-03-10

    Bovie Medical Recalls HNM Disposable Bipolar Ablators Due to Packaging Defect

    Bovie Medical Corporation is recalling 3,862 HNM Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the barrier.

    Product
    HNM Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1163-2021·2021-03-10

    Johnson & Johnson Recalls Nonconforming TECNIS Toric Intraocular Lenses

    Johnson & Johnson Surgical Vision Inc is recalling 27 TECNIS Toric 1-Piece Intraocular Lenses due to the release of nonconforming products.

    Product
    TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1152-2021·2021-03-10

    CooperSurgical Recalls Milex Gellhorn Flexible Pessaries Due to Manufacturing Error

    CooperSurgical is recalling specific lots of Milex Gellhorn Flexible pessaries because they were manufactured with incorrect stem lengths.

    Product
    Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible w/Short Stem Pessary, REF MXKPGSS2-1/4, 2-1/4" (57 mm) with Kit, 2) Gellhorn Flexible w/Short Stem Pessary, REF MXPGSS2-1/4, 2-1/4" (57 mm) without Kit, 3) Gellhorn Flexible w/Short Stem Pessary, REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1162-2021·2021-03-10

    Nihon Kohden Telemetry Recalled for Incorrect Date Stamp or No Data Transfer

    Nihon Kohden America Inc is recalling WMTS Telemetry Receivers because they may display incorrect date stamps or fail to transfer data.

    Product
    WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/ 00841983102561 ORG 9700A/No UDI
    Category
    Medical Device
    Distribution
    46 states
  • LowFDA (Drugs)·D-0289-2021·2021-03-10

    Sun Pharma Recalls Subpotent Cequa Cyclosporine Ophthalmic Solution Vials

    Sun Pharmaceutical Industries is recalling Lot 10007 of Cequa (cyclosporine) ophthalmic solution because the product is subpotent. The recall covers 37,400 cartons distributed nationwide and in Australia.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0298-2021·2021-03-10

    Jubilant Cadista Recalls Methylprednisolone Tablets Due to Illegible Labeling

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Methylprednisolone Tablets USP, 4 MG, due to misaligned printing on the blister card that makes dosing instructions illegible.

    Product
    Methylprednisolone Tablets USP, 4 MG, packaged in a 21-count blister pack, Rx only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-001-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0336-2021·2021-03-10

    Ferrara Candy Company Recalls Assorted Candy Heart Box for Undeclared Ingredients

    Ferrara Candy Company is recalling assorted candy Heart Boxes containing Laffy Taffy, Nerds, and SweeTarts due to undeclared ingredients on the retail packaging.

    Product
    Ferrara Candy Company assorted candy Heart Box, including Laffy Taffy, Nerds, and SweeTarts candies. 10 retail units per wholesale case. Package UPC 0 41420 04965 1
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1168-2021·2021-03-10

    Boston Scientific Recalls Polypectomy Snares Due to Incomplete Pouch Seals

    Boston Scientific is recalling Captivator and Captiflex polypectomy snares because users reported incomplete pouch seals before patient use.

    Product
    Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares. Outer box UPN, Inner Pouch UPN: M00561311 (Box 10), M00561310 M00562301 (Box 10), M00562300; M00562321 (Box 10), M00562320; M00562341 (Box 10), M00562340; M00562451 (Box 10)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1169-2021·2021-03-10

    Boston Scientific Recalls Captivator II Polypectomy Snares Due to Incomplete Seals

    Boston Scientific is recalling Captivator II Single-Use Polypectomy Snares because users reported incomplete pouch seals before use.

    Product
    Captivator II Single-Use Polypectomy Snares Outer box UPN, Inner Pouch UPN: M00561191 (Box 10), M00561190; M00561221 (Box 10), M00561220; M00561222 (Box 20), M00561220; M00561223 (Box 40), M00561220; M00561233 (Box 40), M00561230.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0291-2021·2021-03-10

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium tablets because they contain impurities that exceed FDA specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V150000·2021-03-09

    Autocar Recalls 2020 Legend Vehicles Due to Wiring Harness Defect

    Autocar is recalling 2020 Legend vehicles because a wiring harness may disconnect, causing loss of headlights and wipers. This increases the risk of a crash.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V148000·2021-03-09

    Shyft Group Recalls 2017-2019 Utilimaster Mobile Maintenance Trucks

    Shyft Group is recalling 2017-2019 Utilimaster Mobile Maintenance Trucks equipped with a generator set because a flexible exhaust tube may tear, releasing hot gases and increasing fire risk.

    Product
    UTILIMASTER — UTILIMASTER MOBILE MAINTENANCE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V147000·2021-03-09

    2020-2021 RAM ProMaster City ABS Module Defect Poses Braking Failure Risk

    Chrysler is recalling 2020-2021 RAM ProMaster City vehicles due to potential internal damage to the ABS module, which may cause loss of braking performance. Dealers will replace the module free of charge.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V149000·2021-03-09

    Autocar Recalls 2020-2021 Legend Vehicles for Steering Column Defect

    Autocar is recalling 2020-2021 Legend vehicles because the steering column tilt control cable may contact the steering shaft, potentially causing it to bind and increasing steering effort.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide