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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86826

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

Open FDA event record

Event summary

Timeline bucket
November 13, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Medline Industries 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

5 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 5

Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Z-0779-2021
Recall number
Z-0779-2021
Initiated
November 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
Medline Industries Inc
Quantity
88

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The cylindrical sponge component is not x-ray detectable.

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 cylindrical sponge component is not x-ray detectable.

Code information

Lot 20GBA365 (Expiration 11/30/2024), 20HBM367 (Expiration 11/30/2024), 20IBC934 (Expiration 11/30/2024)

Distribution pattern

Foreign distribution only - Canada.

device · product 2 of 5

Simple Neck Dissection, Model DYNJ47481C - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Z-0780-2021
Recall number
Z-0780-2021
Initiated
November 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
Medline Industries Inc
Quantity
90

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The cylindrical sponge component is not x-ray detectable.

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 cylindrical sponge component is not x-ray detectable.

Code information

Lot 20GBF988 (Expiration 06/30/2024); 20HBM404 (Expiration 06/30/2024); 20JBG876 (Expiration 09/30/2024)

Distribution pattern

Foreign distribution only - Canada.

device · product 3 of 5

Thyroid Pack CKHA-LF, Model DYNJ50352B - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Z-0781-2021
Recall number
Z-0781-2021
Initiated
November 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
Medline Industries Inc
Quantity
40

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The cylindrical sponge component is not x-ray detectable.

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 cylindrical sponge component is not x-ray detectable.

Code information

Lot 20HBM370 (Expiration 02/28/2025); 20IBB678 (Expiration 03/31/2025); 20KBP338 (Expiration Date: 05/31/2025 never distributed)

Distribution pattern

Foreign distribution only - Canada.

device · product 4 of 5

Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Z-0782-2021
Recall number
Z-0782-2021
Initiated
November 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
Medline Industries Inc
Quantity
45

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The cylindrical sponge component is not x-ray detectable.

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 cylindrical sponge component is not x-ray detectable.

Code information

Lot 20FBW645 (Expiration: 02/28/2022); Lot 20HBM397 (Expiration: 02/28/2022)

Distribution pattern

Foreign distribution only - Canada.

device · product 5 of 5

Cardiac Pack - LF, Model DYNJ31903I - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Z-0783-2021
Recall number
Z-0783-2021
Initiated
November 13, 2020
Classification
Class II
Status
Terminated
Recalling firm
Medline Industries Inc
Quantity
360

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The cylindrical sponge component is not x-ray detectable.

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 cylindrical sponge component is not x-ray detectable.

Code information

Lot 20GBG768 (Expiration: 11/30/2021); 20HBO067 (Expiration: 02/28/2022); Lot 20IBC642 (Expiration 03/31/2022)

Distribution pattern

Foreign distribution only - Canada.