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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73465

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

Open FDA event record

Event summary

Timeline bucket
October 05, 2015
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Avid Medical, 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

4 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 4

Convenience Kits, MOHS "OPENING" PROCEDURE TRAY

Z-2589-2016
Recall number
Z-2589-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
240

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

Code information

Catalog No. MCVA0089-04 , LOT# 1010997

Distribution pattern

Recalled product was distributed to 2 states: Virginia and Massachusetts.

device · product 2 of 4

Convenience Kits, MOHS "OPENING" PROCEDURE TRAY

Z-2590-2016
Recall number
Z-2590-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
240

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

Code information

Catalog No. MCVA0089-04 , LOT# 1027144

Distribution pattern

Recalled product was distributed to 2 states: Virginia and Massachusetts.

device · product 3 of 4

PEDIATRIC KIDNEY BIOPSY TRAY

Z-2591-2016
Recall number
Z-2591-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
20

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

Code information

Catalog No. MCVA0091-01 , LOT# 1029428

Distribution pattern

Recalled product was distributed to 2 states: Virginia and Massachusetts.

device · product 4 of 4

MAMMOGRAPHY

Z-2592-2016
Recall number
Z-2592-2016
Initiated
October 05, 2015
Classification
Class II
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
200

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.

Code information

Catalog No. LGHM022-02 , LOT# 1021706

Distribution pattern

Recalled product was distributed to 2 states: Virginia and Massachusetts.