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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 75710

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

Open FDA event record

Event summary

Timeline bucket
October 28, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Integra York PA, 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

Rochester-Pean Hemostatic Forceps 61/4, Curved, Sterile. The Rochester-Pean Hemostatic Forceps 61/4 Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.

Z-0751-2017
Recall number
Z-0751-2017
Initiated
October 28, 2016
Classification
Class II
Status
Terminated
Recalling firm
Integra York PA, Inc
Quantity
150 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
package the sterile instruments may separate causing the packages to open and compromise sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Chevron seals of 6x10 Tyvek peel pouch used to package the sterile instruments may separate causing the packages to open and compromise sterility of the instrument.

Code information

Catalog # ST7-138; lot# 352

Distribution pattern

US Distribution in NC and TX.

device · product 2 of 2

Metzenbaum Scissors 7, Curved, Sterile The Metzenbaum Scissors 7, Curved Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.

Z-0752-2017
Recall number
Z-0752-2017
Initiated
October 28, 2016
Classification
Class II
Status
Terminated
Recalling firm
Integra York PA, Inc
Quantity
50 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
package the sterile instruments may separate causing the packages to open and compromise sterility

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Chevron seals of 6x10 Tyvek peel pouch used to package the sterile instruments may separate causing the packages to open and compromise sterility of the instrument.

Code information

Catalog # ST5-182; lot# 355

Distribution pattern

US Distribution in NC and TX.