The Recall Desk

State

New Jersey product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45801–45825 of 83609

  • ModerateFDA (Drugs)·D-0238-2018·2018-01-31

    Marksans Pharma Recalls Ibuprofen Tablets Due to Odor Complaints

    Marksans Pharma Inc. is recalling 21,584,100 Ibuprofen Tablets, USP 400 mg, due to odor complaints linked to CGMP deficiencies.

    Product
    Ibuprofen Tablets, USP 400 mg, 6 x 3500 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-121-29.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0240-2018·2018-01-31

    Ibuprofen Tablets Recalled for Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling 52,549,000 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide.

    Product
    Ibuprofen Tablets, USP 800 mg, 6 x 1900 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-123-27.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0239-2018·2018-01-31

    Ibuprofen Tablets Recalled Due to Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling specific lots of 600 mg ibuprofen tablets due to odor complaints linked to CGMP deficiencies.

    Product
    Ibuprofen Tablets, USP 600 mg, 6 x 2500 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-122-28.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2018·2018-01-31

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler 45 Instruments

    Intuitive Surgical is recalling 60 da Vinci Xi EndoWrist Stapler 45 instruments due to a manufacturing variation that may prevent the release wrench from unclamping the device.

    Product
    daVinci X EndoWrist(R) Stapler 45, REF 470298 Product Usage: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads, and other Stapler Accessories (including the bladeless obturators) are intended to be used with the da Vinci Surgical System (Model IS4000) for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2018·2018-01-31

    Odan Laboratories Recalls Day Cream SPF15 Due to Stability Failure

    Odan Laboratories is recalling 21 jars of Day Cream SPF15 because the product failed stability specifications at 12 months.

    Product
    Day Cream SPF15 Cr¿me de jour FPS 15, { Avobenzone 2%, Octinoxate 7%, Oxybenzone 5%} 15 ml / 0.5 fl. oz jar. Made in Canada, Kamins Dermatologics Inc. Montreal, Quebec H9R 2Y6. Distributed by Kamins Dermatologics Montreal, Quebec H9R 2Y6 Made in Fabrique au Canada. UPC code 6…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0406-2018·2018-01-31

    Smith & Nephew Recalls Radial Osteotome Blades Due to Incorrect Expiration Dates

    Smith & Nephew is recalling nine Radial Osteotome Blades because the expiration dates on the labels are incorrect. The devices were distributed in the US and Australia.

    Product
    Radial Osteotome Blade, REF 71369314. Used for cutting or preparing bone.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0235-2018·2018-01-31

    Ibuprofen Tablets Recalled for Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling ibuprofen tablets due to odor complaints linked to Current Good Manufacturing Practice (CGMP) deficiencies.

    Product
    IBUPROFEN — IBUPROFEN (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0395-2018·2018-01-31

    Measurement Specialties Reusable Temperature Probes Recalled for Unvalidated Sterilization Instructions

    Measurement Specialties Inc. is recalling 6,076 reusable temperature probes because their sterilization instructions have not been proven through a validation study.

    Product
    Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as Esophageal/Rectal (Adult), Esophageal/Rectal (Pediatric), and Skin (Adult) Intended for use by a licensed physician to continuously monitor human esophageal, rectal, or skin temperature. They are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0230-2018·2018-01-31

    Mylan Recalls Bupropion HCL Extended-Release Tablets Due to Impurities

    Mylan Pharmaceuticals is voluntarily recalling specific bottles of bupropion HCL extended-release tablets due to out-of-specification impurities found during routine stability testing.

    Product
    bupPROPion HCL Extended-Release Tablets, USP (XL) 300 mg, 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC: 0378-2009-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V080000·2018-01-30

    Forest River Recalls 2018 Georgetown RVs Due to Wiring Fire Risk

    Forest River is recalling 2018 Georgetown recreational vehicles because undersized wiring may melt and cause a fire. Dealers will install an additional circuit breaker free of charge.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V082000·2018-01-30

    Audi Recalls Vehicles Due to Driver Air Bag Inflator Explosion Risk

    Volkswagen Group of America is recalling specific Audi models because the driver's air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    AUDI — AUDI S5 CABRIOLET, S4 CABRIOLET, A3, A4 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V077000·2018-01-30

    Entegra Recalls Aspire and Insignia Motorhomes Due to Brake Reservoir Defect

    Entegra is recalling 2015-2018 Aspire and Insignia motorhomes because the air brake supply reservoir is undersized, which may reduce braking performance and increase crash risk.

    Product
    ENTEGRA — ENTEGRA INSIGNIA, ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E007000·2018-01-30

    Lippert Components Recalls Ford F53 Chassis for Driveshaft Misalignment

    Lippert Components is recalling specific Ford F53 chassis used in Coachmen and Mirada RVs because a misaligned driveshaft may cause excessive vibration and potential vehicle disablement.

    Product
    STRUCTURE:FRAME AND MEMBERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V083000·2018-01-30

    Thomas Built Buses Recall Fire Extinguishers Due to Clogging and Injury Risk

    Daimler Trucks North America is recalling 2002-2017 Thomas Built Buses equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, FS-65, SAF-T-LINER C2, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V079000·2018-01-30

    Eclipse Recalls 2019 Attitude Trailers Due to Incorrect Tire Load Range

    Eclipse Recreational Vehicles is recalling 2019 Attitude trailers equipped with tires that have the incorrect load range, which may lead to tire failure and increase crash risk.

    Product
    ECLIPSE — ECLIPSE ATTITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18086·2018-01-30

    Walgreens Pain and Itch Relief Cream Recalled for Packaging Safety

    Natureplex is recalling Well at Walgreens pain and itch relief cream because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Well at Walgreens pain and itch relief cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V078000·2018-01-30

    Jayco Recalls 2017 Precept Motorhomes Due to Brake Fluid Leak Risk

    Jayco is recalling 2017 Precept motorhomes because missing valve block ball plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    JAYCO — JAYCO PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V072000·2018-01-29

    Jayco Eagle Travel Trailer Recall for Underrated Safety Chains

    Jayco is recalling 2017-2018 Eagle 333BHOK travel trailers because the safety chains are rated below the vehicle's weight limit, posing a crash risk if the trailer detaches.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V076000·2018-01-29

    Harley-Davidson Recalls ABS Motorcycles Due to Brake Fluid Deposits

    Harley-Davidson is recalling 2008-2011 ABS-equipped motorcycles because brake fluid deposits may cause the ABS valve to stick, reducing braking ability and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTP, VRSCF, VRSCDXA, VRSCDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V075000·2018-01-29

    Jayco Recalls 2018 Eagle Travel Trailers Due to Stove Gas Leak Risk

    Jayco is recalling 2018 Eagle travel trailers because the furnace can cause the cooktop flame to go out while gas continues to flow, creating an explosion risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V073000·2018-01-29

    Jayco Recalls 2018 Eagle Travel Trailers for Incorrect Weight Labeling

    Jayco is recalling 2018 Eagle travel trailers because the Gross Vehicle Weight Rating label may be incorrect, potentially allowing the vehicle to be overloaded.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18T001000·2018-01-29

    Vogue Tyre & Rubber Recalls Signature V Tires for Missing Date Codes

    Vogue Tyre & Rubber is recalling specific Signature V tires because they lack date codes on the sidewall, which may prevent owners from identifying recalled tires.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide