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Recall Observatory FDA recall evidence

Device product

Robotics Pack, REF SJVO56B

Z-0178-2024

September 01, 2023

Class II

Product summary

Firm
American Contract Systems, Inc.
Event
Event 93086
Status
Ongoing
Classification
Class II
Quantity
112 cases
Official record key
device-enforcement:Z-0178-2024

Official wording

Reason: During an internal investigation, ACS identified that the components, I.V. Cath (part number 4252535-02) and Adhesive Dermabond (part number DHVM12) were inadvertently subjected to the ACS sterilization process and exposed to EO and higher temperatures than approved by the component manufacturer. As a result, the components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) have higher than specified EO residuals.

Code information: UDI/DI 00191072122339, Lot Numbers: 965231

Distribution pattern: US Nationwide distribution in the states of FL, IA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    During an internal investigation, ACS identified that the components, I.V. Cath (part number 4252535-02) and Adhesive Dermabond (part number DHVM12) were inadvertently subjected to the ACS sterilization process and exposed to EO and higher temperatures than approved by the component manufacturer. As a result, the components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) have higher than specified EO residuals.

Field note

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