The Recall Desk

State

California product recalls

72,940 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,245
Critical
1,605
Severe
2,843
Most recent
2026-09-09

Of the 13,245 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,843 (21%) are Severe.

These figures cover only the 13,245 recalls whose distribution notice names California specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4026–4050 of 86185

  • ModerateFDA (Food)·H-0378-2026·2026-01-14

    Gourmet kunafe pastry recalled because it may contain partially hydrogenated oils

    Ziyad Brothers Importing is recalling 575 cases of Baraka Gourmet Pastry Kunafe because the product may contain partially hydrogenated oils.

    Product
    Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0377-2026·2026-01-14

    French style puff pastry recalled because it may contain partially hydrogenated oils

    Ziyad Brothers Importing is recalling 2,865 cases of Baraka French Style Puff Pastry because the product may contain partially hydrogenated oils.

    Product
    Baraka French Style Puff Pastry 1lb and 1.5lbs sizes, UPCs 8 22514 28540 3 and 8 22514 28550 2, both sizes 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1010-2026·2026-01-14

    Laparoscopic trocars recalled over a potentially extended blade obturator length

    Applied Medical Resources is recalling 450 units of the Kii Low Profile Bladed Dual Pack because of the potential for extended length of the blade obturator after assembly.

    Product
    Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1036-2026·2026-01-14

    Intracranial pressure monitoring kits recalled over corrosion stains on the needle

    Integra LifeSciences is recalling 1,301 Codman Microsensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.

    Product
    Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1025-2026·2026-01-14

    DxI 600 immunoassay analyzers recalled over a failure to restart after shutdown

    Beckman Coulter is recalling 1,272 UniCel DxI 600 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.

    Product
    Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260; Immunoassay Method, Troponin Subunit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0255-2026·2026-01-14

    Oxycodone and acetaminophen 7.5 mg tablets recalled over a missing imprint

    SpecGx is recalling 74,544 bottles of Oxycodone and Acetaminophen CII Tablets, 7.5 mg/325 mg, because of the potential for the imprint to be missing on tablets.

    Product
    OXYCODONE AND ACETAMINOPHEN — OXYCODONE AND ACETAMINOPHEN (OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1037-2026·2026-01-14

    CereLink pressure sensor kits recalled over corrosion stains on the needle

    Integra LifeSciences is recalling 5,116 Codman CereLink ICP Sensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.

    Product
    Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink ICP Sensor Basic Kit consists of the CereLink ICP Sensor (ICP Sensor) and a 14-gauge Tuohy needle with stylet. The ICP Sensor is a nylon tube with a microminiature strain gauge pressure transduc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26E002000·2026-01-13

    Lippert Recalls 3000 Series Hidden Hinge Ramp Doors for Breakage Risk

    Lippert is recalling 3000 Series Hidden Hinge Ramp Doors because they may break away from the frame during use, increasing the risk of injury.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V006000·2026-01-12

    Terex Recalls 2025 Aerial Devices Due to Hydraulic Overheating Risk

    Terex is recalling 2025 TL, LT, LTM40, HR40, HR46, and SCM55 aerial devices because a control valve defect may cause hydraulic equipment to overheat, posing a burn risk.

    Product
    TEREX — TEREX TL-SERIES, HR40, HR46, LT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V005000·2026-01-09

    Land Rover Recalls 2026 Range Rover Sport for Incorrect Weight Label

    Jaguar Land Rover is recalling 2026 Range Rover Sport vehicles because the certification label lists incorrect weight information, which could lead to overloading.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26166·2026-01-08

    Leaf vacuums recalled after loose pieces were ejected from the units

    About 60,250 DR Power walk-behind and tow-behind leaf vacuums are being recalled because pieces can come loose inside the unit or debris can pierce the chute, ejecting material.

    Product
    Walk-Behind Leaf Vacuums and Tow-Behind Leaf Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26172·2026-01-08

    Rattan six-drawer dressers recalled over tip over and entrapment hazards

    About 870 Rattan 6-Drawer Dressers, model YD001, are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.

    Product
    Rattan 6-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26171·2026-01-08

    NFSVLB baby bath seats recalled over tip over and entrapment hazards

    About 1,430 NFSVLB baby bath seats are being recalled because they are unstable, can tip over, and have leg openings that allow a child's torso to become entrapped.

    Product
    NFSVLB Baby Bath Seats (blue)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26169·2026-01-08

    Braided crib bumpers recalled under the federal crib bumper ban

    About 55 SARO Braided Crib Bumpers, Model 1374, are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.

    Product
    SARO Braided Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26176·2026-01-08

    Wooden pounding toys recalled over high-powered magnets that can detach

    About 3,500 Lterfear Multifunction Pounding Games are being recalled because they contain high-powered magnets that can detach, posing an ingestion hazard to children.

    Product
    Lterfear Multifunction Pounding Game
    Category
    Consumer Product
    Distribution
    Distributed nationwide