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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82271

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 18, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Avitus Orthopaedics, Inc.

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

2 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 2

Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-110 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow

Z-1046-2019
Recall number
Z-1046-2019
Initiated
February 18, 2019
Classification
Class II
Status
Terminated
Recalling firm
Avitus Orthopaedics, Inc.
Quantity
508 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Breach in the sterile barrier

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breach in the sterile barrier pouch may compromise sterility of the device.

Code information

Lot Number/Exp. Date Z2458218A 2018-05-01; Z2458253B 2018-05-01; Z2458379B 2018-10-01; Z2458448B 2019-01-01

Distribution pattern

US Nationwide distribution to states of: AZ, CA, CT, FL, MD, MI, NM, OH and PA; and Internationally to: Brazil.

device · product 2 of 2

Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-210 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow

Z-1047-2019
Recall number
Z-1047-2019
Initiated
February 18, 2019
Classification
Class II
Status
Terminated
Recalling firm
Avitus Orthopaedics, Inc.
Quantity
207 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Breach in the sterile barrier

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breach in the sterile barrier pouch may compromise sterility of the device.

Code information

Lot Number/Exp. Date Z2458287A 2018-06-01; Z2458379A 2018-10-01

Distribution pattern

US Nationwide distribution to states of: AZ, CA, CT, FL, MD, MI, NM, OH and PA; and Internationally to: Brazil.