The Recall Desk

Hazard

Resterilization recalls

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

What the numbers show

Total
42
Critical
0
Severe
0
Most recent
2025-10-22

Of the 42 resterilization 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 resterilization 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.

26–42 of 42

  • 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-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 (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-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 (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 (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-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-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 (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 (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-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 (Devices)·Z-2263-2025·2025-08-13

    Robotic uro/gyn packs contain an inadvertently resterilized visualization system

    Robotic Uro/Gyn Pack medical convenience kits are being recalled because the Clearify Visualization System inside was inadvertently resterilized, causing discoloration. 372 units are affected.

    Product
    ROBOTIC URO/GYN PACK. Medical convenience kit.
    Category
    Medical Device
    Distribution
    7 states