The Recall Desk

State

New Jersey product recalls

72,907 recalls have nationwide distribution and so reach New Jersey. 9,759 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,759
Critical
1,249
Severe
2,482
Most recent
2026-09-09

Of the 9,759 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 2,482 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,759 recalls whose distribution notice names New Jersey specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1501–1525 of 82666

  • SevereFDA (Devices)·Z-2249-2026·2026-06-10

    BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0910-2026·2026-06-10

    Cold prep cream sauce contains dry milk recalled for Salmonella

    Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2224-2026·2026-06-10

    Ivenix infusion pumps may hide internal damage after being dropped

    Ivenix Infusion System Large Volume Pumps are being recalled because dropping or jarring can loosen the touchscreen input cable, causing random touches or an unresponsive screen.

    Product
    Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Devices)·Z-2276-2026·2026-06-10

    B. Braun spinal needle kits recalled over Huons bupivacaine quality issues

    Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.

    Product
    Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2256-2026·2026-06-10

    BD spinal trays recalled as a sub-recall of Huons bupivacaine

    BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2257-2026·2026-06-10

    BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0903-2026·2026-06-10

    Birch Benders sweet potato pancake and waffle mix contains undeclared egg

    Birch Benders Sweet Potato Pancake and Waffle Mix, 12 oz, is being recalled because of undeclared egg. The recall covers 5,340 cases.

    Product
    Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Devices)·Z-2255-2026·2026-06-10

    BD Whitacre spinal trays across nine catalog numbers recalled over bupivacaine

    BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2250-2026·2026-06-10

    BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0908-2026·2026-06-10

    Aramark cheese sauce contains dry milk powder recalled over Salmonella

    Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2254-2026·2026-06-10

    BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2026·2026-06-10

    BD Quincke spinal trays recalled over Huons bupivacaine quality issues

    BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2277-2026·2026-06-10

    Spinocan spinal needle kits recalled over Huons bupivacaine quality issues

    Spinocan spinal needle procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall. 16,080 units affected.

    Product
    Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2309-2026·2026-06-10

    Sharpoint microsurgical knives labeled 2.2mm actually measure 3.0mm

    Sharpoint 2.2 mm angled double-bevel microsurgical knives are being recalled because 3.0 mm knives were labeled and packaged as 2.2 mm. 1,818 units affected.

    Product
    Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2297-2026·2026-06-10

    BD Pyxis MedStation 4000 fingerprint scanner may overheat and burn

    The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation 4000 REF: 303 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0896-2026·2026-06-10

    Straus Family Creamery Dutch chocolate ice cream may contain metal

    Straus Family Creamery Dutch Chocolate Organic Super Premium Ice Cream in quarts is being recalled over potential contamination with foreign objects, specifically metal pieces.

    Product
    STRAUS FAMILY CREAMERY Dutch Chocolate ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100122
    Category
    Food
    Distribution
    17 states
  • HighFDA (Food)·H-0982-2026·2026-06-10

    Pavilions single serve banana nut muffins do not declare walnut

    Pavilions Banana Nut Muffins single serve, an Albertsons store-made item, are being recalled because the contains statement does not declare walnut. 55 units are affected.

    Product
    UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1016-2026·2026-06-10

    Albertsons Waldorf salad does not declare walnut allergen

    Albertsons store-made Ready Meals Salad Waldorf is being recalled because the contains statement does not declare walnut. 82 units are affected.

    Product
    UPC 21163600000 Ready Meals SALAD WALDORF SS This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1031-2026·2026-06-10

    Albertsons lox avocado toast does not declare salmon allergen

    Albertsons store-made Lox Avocado Toast is being recalled because the contains statement does not declare salmon. 19 units are affected.

    Product
    UPC 21299900000 LOX AVOCADO TOAST FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2304-2026·2026-06-10

    BD Pyxis MedBank Mini fingerprint scanner may overheat and burn

    The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0554-2026·2026-06-10

    Spectra lidocaine ampules recalled over lack of sterility assurance

    Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0573-2026·2026-06-10

    H-E-B extra strength antacid tablets contain small metallic particles

    H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HEB EXTRA STREGTH ANTACID — HEB EXTRA STREGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2293-2026·2026-06-10

    Arvis Hip and Knee 2.0 trackers may show wear and corrosion

    Arvis Hip & Knee 2.0 Instrument Sets are being recalled because the Impactor V-Block Assembly and Trackers may show early wear or corrosion on the exposed magnet face.

    Product
    Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1030-2026·2026-06-10

    Chewie Susans thumbprint cookie snack platters do not declare pecan

    Albertsons store-made Platter Snack Chewie Susans Thumbprints is being recalled because the contains statement does not declare pecan. 158 units are affected.

    Product
    UPC 22304700000 PLATTER SNACK CHEWIE SUSANS THUMBPRINTS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide