Parks Medical Electronics, Inc Recall: Devices includes a Multi Port Inflator or without M
Parks Medical Electronics, Inc Recall: Devices includes a Multi Port Inflator or without M is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Parks Medical Electronics, Inc; Product: Devices includes a Multi Port Inflator or without Multi Port Inflator (MPI). All the devices are vascular
| Recalling firm | Parks Medical Electronics, Inc |
|---|---|
| Product | Devices includes a Multi Port Inflator or without Multi Port Inflator (MPI). All the devices are vascular blood flow machines. Devices are distributed with pressure cuffs of varying sizes as accessories. Affected models include *2100-SX, 3000 series, 2017, 2016, 2015, 2014, 1059, 1059-A, *1059-C, *1058-C, 4000 series, 1100 series, 1060 series, 1080 series, 234 and 246. (* = current production model) All the devices are used in the study and diagnosis of vascular disease and blockages in the upper and lower extremities. |
| Reason for recall | Parks Medical Electronics, Inc. was made aware of two incidents where an air supply tube from their PARKS PVR unit was inadvertently connected to an IV in the patient's arm instead of into the blood pressure cuff. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide distribution: USA (nationwide) and countries of: Australia, Brazil, Canada, Chile, Egypt, Germany, Greece, Hong Kong, India, Israel, Italy, Japan, Korea, Mexico, Peru, Republica Argentina, Spain, Switzerland, and Venezuela. |
| Recall initiated | 20120808 |
| Recall number | Z-0443-2013 |
| Category | device |
| State | OR |
| Country | United States |
$29/mo
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