The Recall Desk

Hazard

Class Ii recalls

1,428 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,428
Critical
0
Severe
0
Most recent
2026-07-08

Of the 1,428 class ii recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all class ii recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1101–1125 of 1428

  • ModerateFDA (Food)·H-0403-2025·2025-08-13

    Clover Valley vitamin D whole milk recalled after a temperature excursion

    Clover Valley Vitamin D Whole Milk in gallon and half gallon jugs is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 43 units affected.

    Product
    1) Clover Valley Vitamin D Whole Milk, 1 GAL (3.78 L), packaged in a plastic jug, UPC: 070744002196 2) Clover Valley Vitamin D Whole Milk, 1/2 GAL (1.89 L), packaged in a plastic jug, UPC: 070744009645
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2247-2025·2025-08-13

    General laparoscopy trays contain an inadvertently resterilized visualization system

    General Laparoscopy Tray medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 574 units are affected.

    Product
    GENERAL LAPAROSCOPY TRAY. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0416-2025·2025-08-13

    Velveeta sharp cheddar slices recalled after a shipping trailer temperature excursion

    Velveeta Slices Sharp Cheddar, 16 count, are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Velveeta Slices Sharp Cheddar, 16 ct., NET WT 12 OZ (340g), packaged in plastic/cardboard, UPC: 021000044894
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2243-2025·2025-08-13

    daVinci urology and prostate packs contain a resterilized visualization system

    DA VINCI PACK URO/PROSTATE medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 21 units affected.

    Product
    DA VINCI PACK URO/PROSTATE. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0418-2025·2025-08-13

    Yoplait strawberry banana yogurt recalled after a shipping trailer temperature excursion

    Yoplait Original Strawberry Banana Yogurt, 6 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units are affected.

    Product
    Yoplait Original Strawberry Banana Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003136
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2256-2025·2025-08-13

    Laparoscopy packs contain an inadvertently resterilized visualization system

    Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 452 units are affected.

    Product
    LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0408-2025·2025-08-13

    Minute Maid fruit punch recalled after a shipping trailer temperature excursion

    Minute Maid Fruit Punch, 59 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 4 units are affected.

    Product
    Minute Maid Fruit Punch, 59 FL OZ (1.8 QT) 1.75 L, packaged in a paper carton, UPC: 025000047732
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0412-2025·2025-08-13

    Shamrock Farms whole milk recalled after a shipping trailer temperature excursion

    Shamrock Farms Whole Milk, 12 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units are affected.

    Product
    Shamrock Farms Whole Milk, 12 FL OZ (354 ML), packaged in a plastic bottle, UPC: 028300000896
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2254-2025·2025-08-13

    Laparoscopic GYN kits contain an inadvertently resterilized visualization system

    Laparoscopic GYN medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 18 units are affected.

    Product
    LAPAROSCOPIC GYN. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·H-0417-2025·2025-08-13

    Yoplait Harvest Peach yogurt recalled after a shipping trailer temperature excursion

    Yoplait Original Harvest Peach Yogurt, 6 oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Yoplait Original Harvest Peach Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003075
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2253-2025·2025-08-13

    Lap chole packs contain an inadvertently resterilized visualization system

    Lap Chole Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 85 units are affected.

    Product
    LAP CHOLE PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2249-2025·2025-08-13

    GS endoscopy packs contain an inadvertently resterilized visualization system

    GS Endoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 816 units are affected.

    Product
    GS ENDOSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2245-2025·2025-08-13

    daVinci urology kits contain an inadvertently resterilized visualization system

    DAVINCI UROLOGY medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 166 units are affected.

    Product
    DAVINCI UROLOGY. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2257-2025·2025-08-13

    LAVH packs contain an inadvertently resterilized visualization system

    LAVH Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 292 units are affected.

    Product
    LAVH PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2267-2025·2025-08-13

    DxI 800 immunoassay analyzer motor current resets below the required setting

    A DxI 800 Access Immunoassay Analyzer is being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results.

    Product
    DxI 800 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71457
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0401-2025·2025-08-13

    Clover Valley 2% reduced fat milk recalled after a temperature excursion

    Clover Valley 2% Reduced Fat Milk in gallon and half gallon jugs is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 13 units affected.

    Product
    1) Clover Valley 2% Reduced Fat Milk, 1 GAL (3.78 L), packaged in a plastic jug, UPC: 070744002202 2) Clover Valley 2% Reduced Fat Milk, 1/2 GAL (1.89 L), packaged in a plastic jug, UPC: 070744009652
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2250-2025·2025-08-13

    GYN laparoscopy packs contain an inadvertently resterilized visualization system

    GYN Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 346 units are affected.

    Product
    GYN LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0571-2025·2025-08-13

    Xolair auto-injectors exposed to temperatures outside labeled storage requirements

    Xolair (omalizumab injection) 150 mg/mL auto-injectors are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 6 units affected.

    Product
    XOLAIR — XOLAIR (OMALIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2246-2025·2025-08-13

    General laparoscopy packs contain an inadvertently resterilized visualization system

    Gen Laparoscopy Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 321 units are affected.

    Product
    GEN LAPAROSCOPY PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2237-2025·2025-08-13

    BD Trucount 664343 control kits carry incorrect standard deviation values

    BD Trucount Controls 30 Test kits, REF 664343, are being recalled because they contain incorrect standard deviation values for the low and high control beads. 10 kits are affected.

    Product
    BD Trucount Controls, 30 Test - REF: 664343, RxOnly, IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2241-2025·2025-08-13

    Cardiac robot packs contain an inadvertently resterilized visualization system

    Cardiac Robot Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 20 units are affected.

    Product
    CARDIAC ROBOT PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0573-2025·2025-08-13

    Recombinate antihemophilic factor vials exposed to temperatures outside labeled storage

    Recombinate [Antihemophilic Factor (Recombinant)] 5 mL vials are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 3 units affected.

    Product
    RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2269-2025·2025-08-13

    UniCel DxI 600 analyzer motor current resets below the required setting

    UniCel DxI 600 Access Immunoassay Analyzers are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors. 271 systems are affected.

    Product
    UniCel DxI 600 Access Immunoassay Analyzer, Part Number A30260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2266-2025·2025-08-13

    UniCel DxI 800 analyzer motor current resets below the required setting

    UniCel DxI 800 Access Immunoassay Analyzers are being recalled because software overwrites the factory PnP X-motor current setting, causing increased motion errors that could delay patient results. 2,203 systems affected.

    Product
    UniCel DxI 800 Access Immunoassay Analyzer, Part Number 973100
    Category
    Medical Device
    Distribution
    Distributed nationwide