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Recall company profile

Avid Medical, Inc. Recalls

Overview of recall records associated with Avid Medical, Inc., including dates, categories and classifications where available.

132recall records

Sep 16, 2026latest record date

Mar 7, 2018earliest record date

Recall history in this database

Classification mix: Class II: 115, Class I: 17.

Medical DeviceJun 16, 2021

Avid Medical FISTULA ON-OFF KIT recall — FDA Z-1785-2021

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…

Class IFDA: TerminatedAvid Medical, Inc.

Medical DeviceJun 16, 2021

Avid Medical DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03 recall — FDA Z-1787-2021

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…

Class IFDA: TerminatedAvid Medical, Inc.

Medical DeviceJun 16, 2021

Avid Medical ADULT CHEST TUBE TRAY recall — FDA Z-1784-2021

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…

Class IFDA: TerminatedAvid Medical, Inc.

Medical DeviceJun 16, 2021

Avid Medical FISTULA (ON/OFF) ALL IN ONE BAG recall — FDA Z-1786-2021

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…

Class IFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1517-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1521-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1523-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1518-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1515-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1522-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1520-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1519-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 25, 2020

Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1516-2020

The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom DAVINCI PACK convenience kits, Item Code: ADVU037-09 recall — FDA Z-0780-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits, Item Code: MADN011-02 recall — FDA Z-0791-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom GENERAL PACK convenience kits, Item Code: LGHM041-06 and LGHM041-08 recall — FDA Z-0789-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom SHOULDER ARTHROSCOPY convenience kits, Item Code: MADN010-02 recall — FDA Z-0800-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom MINOR PROCEDURE 6A convenience kits, Item Code: MADN032-01 recall — FDA Z-0794-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom NEURO PK convenience kits, Item Code: LGHM021-08 recall — FDA Z-0795-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom EXTREMITY PACK convenience kits, Item Code: MADN012-01 and MADN012-02 recall — FDA Z-0788-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom OBSTETRICAL PACK convenience kits, Item Code: HLDH008-04 recall — FDA Z-0782-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom PLASTIC BASIN PACK convenience kits, Item Code: MADN008-03 recall — FDA Z-0798-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom PACEMAKER PACK convenience kits, Item Code: LGHM030-06 recall — FDA Z-0796-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Medical DeviceMar 7, 2018

AVID TruCustom ORTHO TRAY convenience kits, Item Code: LGHM004-07 and LGHM004-08 recall — FDA Z-0785-2018

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Class IIFDA: TerminatedAvid Medical, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Avid Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.