The Recall Desk

Hazard

Device Detachment recalls

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

What the numbers show

Total
51
Critical
1
Severe
22
Most recent
2026-07-15

Of the 51 device detachment recalls we have scored against our rubric, 1 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 22 (43%) 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 device detachment 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.

51–51 of 51

  • SevereFDA (Devices)·Z-0672-2013·2013-01-23

    Bausch and Lomb Amvisc Cannulas Recalled for Detachment Risk

    Bausch and Lomb is recalling Amvisc and Amvisc Plus cannulas that may detach from syringes during injection, posing a risk of serious patient injury.

    Product
    Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model 59051, 59081, 59051L, 59081L) and Amvisc Plus 1.6% Sodium Hyaluronate (Model 60081, 60051, 60051L, 60081L) ophthalmic viscosurgical device. The 27G disposable cannula is a
    Category
    Medical Device
    Distribution
    2 states