RecallRadar

FDA Device recall Z-1506-2018

T4 Zipper Toga, (L/XL)

On 2018-05-02 the FDA classified a Class II recall of T4 Zipper Toga, (L/XL) by Stryker Instruments Div, citing separation of material layers may occur, causing a potential risk of exposure to contaminants.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1506-2018
ClassificationClass II
Statusterminated
Initiated2018-02-23
Published2018-05-02
Last updated2026-09-13 11:54 UTC
CompanyStryker Instruments Div
DistributionUS

Product

T4 Zipper Toga, (L/XL); Catalog Number: 0400-820-000 Sterile personal protection garment

Reason

Separation of material layers may occur, causing a potential risk of exposure to contaminants.

Identifiers

code_info
Lot numbers: 17061810, 17061814, 17071878, 17071903, 17071918, 17071920, 17071949, 17071960, 17071970, 17071974, 170719…Lot numbers: 17061810, 17061814, 17071878, 17071903, 17071918, 17071920, 17071949, 17071960, 17071970, 17071974, 17071997, 17072002, 17072006, 17072016, 17102897, 17102926, 17102936, 17102942, 17102956, 17102971, 17102994, 17102996, 17113021, 17113034, 17113037, 17113084, 17113133, 17113191, 17113197, 17113203, 17113221

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1506-2018%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.