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ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.

FDA Device Recall #Z-2822-2015 — Class II — June 12, 2015

Recall Summary

Recall Number Z-2822-2015
Classification Class II — Moderate risk
Date Initiated June 12, 2015
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm MicroAire Surgical Instruments, LLC
Location Charlottesville, VA
Product Type Devices
Quantity 168, ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump

Product Description

ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.

Reason for Recall

There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.

Distribution Pattern

Nationwide Distribution.

Lot / Code Information

Serial numbers 14101241, 4091238, 15011258, 15051279, 13101158, 15051275, 14021190, 12121111, 15051274, 14071221, 13081149, 13031123, 14021187, 14121254, 14081231, 13121173, 13111167, 13101164, 13121172, 14091234, 14111248, 14031196, 13061142, 15031264, 13121171, 13021116, 15051276, 13041131, 13101160, 14051210, 15041271, 14071222, 14051208, 15021260, 13111166, 13101163, 14111246, 13111168, 13101158, 14061212, 13081152, 13121177, 13061145, 15051280, 15061283, 14041200, 13021114, 14011184, 14031193, 13111165, 14011182, 14111249, 14101242, 14011181, 15041272, 13101156, 13041126, 14101240, 14021188, 12111108, 13061141, 12121112, 13061140, 13041128, 13081150, 14031195, 15051281, 14031197, 14081228, 14101243, 14031199, 14081232, 14071226, 13081148, 14111244, 14091238, 15051279, 13091154, 13121179, 14121252, 15041268, 14071225, 14071223, 15031266, 13031122, 13061144, 14021186, 14091233, 13101161, 14031194, 15041273, 13121170, 13021120, 13011113, 13121174, 14041201, 15021261, 14011183, 13061143, 13121175, 15021262, 15011259, 13101157, 14071227, 13091155, 13111169, 14121251, 14061211, 14071216, 14041207, 13041124, 14021189, 14011185, 14031198, 12101105, 14071224, 14041203, 14071220, 13051132, 14091239, 15041269, 14051209, 15021263, 15011257, 13081147, 13031121, 14101241, 15011258, 13041125, 13081151, 13101159, 13121176, 12121109, 14061213, 13121178, , 13101162, 14111245, 13061138, 14081229, 14021192, 14091237, 14121253, 13061139, 14121255, 15051278, 15051277, 14071217, 15011256, 13021118, 13071146, 13051135, 13051136, 13051137, 14071219, 14081230, 13041127, 12101106, 14061215, 12101107, 14061214, 15041267, 14041206, 14041202, 13041130, 13041129, 14021191, 13051133, 13051134, 14011180, 14091235, 14091236, 14111247, and 14111250.

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Z-0412-2018 Class II SST TWIST DRILL, STANDARD, 1.6mm Dia. x 127mm, ... May 22, 2017
Z-1407-2017 Class II MicroAire K-Wires Feb 21, 2017

Frequently Asked Questions

Contact your physician immediately if you use an electrical device or implant affected by this recall. For external devices (monitors, pumps), stop using the device and contact the manufacturer for a replacement. For implanted devices (pacemakers, ICDs), your cardiologist will assess whether you need device replacement surgery — the decision depends on how dependent you are on the device and the actual failure rate observed in the field. Do not attempt to repair or modify a recalled electrical medical device yourself. Monitor for any new or unusual symptoms and report them to your doctor.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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