Exact FDA event identifier

Event 76156

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: December 22, 2016
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Flower Orthopedics Corporation

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.

Z-1113-2017

Recall number: Z-1113-2017
Initiated: December 22, 2016
Classification: Class II
Status: Terminated
Recalling firm: Flower Orthopedics Corporation
Quantity: N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The product is being recalled due to incidence and reports of the product breaking during surgery.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product is being recalled due to incidence and reports of the product breaking during surgery.

Code information

Device Listing: D267957

Distribution pattern

Distributed throughout the United States