RecallRadar

FDA Device recall Z-3153-2026

Haylard BASIC BIOPSY TRAY

On 2026-09-23 the FDA classified a Class I recall of Haylard BASIC BIOPSY TRAY by Avid Medical, citing potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3153-2026
ClassificationClass I
Statusongoing
Initiated2026-08-10
Published2026-09-23
Last updated2026-09-29 05:30 UTC
CompanyAvid Medical
DistributionIL, NC, VA, WY

Product

Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;

Reason

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Identifiers

code_info
Model/Item Number (Kit): PM415; UDI-DI: 10809160322154; Kit Lots: 1652485, 1656642, 1667835, 1676219, 1682251, 1691940;…Model/Item Number (Kit): PM415; UDI-DI: 10809160322154; Kit Lots: 1652485, 1656642, 1667835, 1676219, 1682251, 1691940; Recalled Sodium Chloride Ampule Lot: AB5002, AB4003;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-29 05:30 UTC. Current status: ongoing.

Other recalls by Avid Medical

All Avid Medical recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3153-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.