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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87720

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

Open FDA event record

Event summary

Timeline bucket
April 09, 2021
Product types
Device
Classifications
Class I
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

ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04

Z-1784-2021
Recall number
Z-1784-2021
Initiated
April 09, 2021
Classification
Class I
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
130 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
package integrity. A breach

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

Code information

Part Number: LAKC001-04; Package GTIN: 20809160261016; Lot Number: 1404809 (Expiration Date: 08/01/2021) and 1408337 (Expiration Date: 09/01/2021) Part Number: LAKC001-04; Package GTIN: 20809160293130; Lot Number: 1427628 (Expiration Date: 09/01/2021) Part Number: LAKC001-04; Package GTIN: 20809160313005; Lot number: 1427629 (Expiration Date: 09/01/2021), 1432814 (Expiration Date: 11/30/2021), and 1436046 (Expiration Date: 11/30/2021)

Distribution pattern

Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN

device · product 2 of 4

FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.

Z-1785-2021
Recall number
Z-1785-2021
Initiated
April 09, 2021
Classification
Class I
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
720 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
package integrity. A breach

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

Code information

Part Number: MMTN020; Package GTIN: 20809160223489; Lot Number: 1351695 (Expiration Date: 10/31/2021)

Distribution pattern

Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN

device · product 3 of 4

FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03

Z-1786-2021
Recall number
Z-1786-2021
Initiated
April 09, 2021
Classification
Class I
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
160 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
package integrity. A breach

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

Code information

Part Number:VAMK024-03; Package GTIN: 20809160342500; Lot Number: 1445301 (Expiration Date: 04/30/2022) and 1445302 (Expiration Date: 04/30/2022)

Distribution pattern

Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN

device · product 4 of 4

DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.

Z-1787-2021
Recall number
Z-1787-2021
Initiated
April 09, 2021
Classification
Class I
Status
Terminated
Recalling firm
Avid Medical, Inc.
Quantity
560 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
package integrity. A breach

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Environmental control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

Code information

Part Number:VMED004-03; Package GTIN: 20809160238247; Lot Number: 1409970 (Expiration Date: 04/26/2022), 1412734 (Expiration Date: 10/01/2021), 1413146 (Expiration Date: 10/01/2021), and 1413395 (Expiration Date: 04/25/2022)

Distribution pattern

Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN