FDA Device recall Z-0814-2016
Jadak Barcode Scanner, Part No. 350587-32, 350587-41, 351377-32
- FDA Device
- Class II
- terminated
- Published 2016-02-24
On 2016-02-24 the FDA classified a Class II recall of Jadak Barcode Scanner, Part No. 350587-32, 350587-41, 351377-32 by Carefusion 303, citing customers reported issues when scanning medications with the scanners. When a user scans a medication using the affected barcode scanner, information on a different medication cou….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0814-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-15 |
| Published | 2016-02-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Jadak Barcode Scanner, Part No. 350587-32, 350587-41, 351377-32. Product Usage: An accessory for the Pyxis Anesthesia ES system and Pyxis Anesthesia system 4000 stations. The Jadak Barcode Scanner is used to scan medication labels during refill of the Pyxis Anesthesia ES system and Pyxis Anesthesia system 4000 stations and dispensing medication for patients.
Reason
Customers reported issues when scanning medications with the scanners. When a user scans a medication using the affected barcode scanner, information on a different medication could be communicated to the Pyxis product.
Identifiers
| code_info | 14488129 14488133 14488134 14463683 14463684 14463687 14463688 14463689 14463690 14463691 14463692 14463693…14488129 14488133 14488134 14463683 14463684 14463687 14463688 14463689 14463690 14463691 14463692 14463693 14463694 14463695 14463696 14463697 14463698 14463700 14463701 14463702 14463703 14463704 14463707 14463708 14463709 14463710 14463711 14463712 14463713 14463714 14463715 14463716 14463717 14467646 14467647 14513579 13941887 13941888 13941889 13941890 13941891 13941892 13941893 13941894 13941895 13941896 13941897 13941898 13941899 13943819 13943820 13972753 14474968 14510555 14510556 14510165 14510164 14510494 14510495 14510557 14510559 14510561 14510563 14510564 14510565 14510569 14510570 14510571 14510572 14454894 14477691 14477692 14477693 14477694 14477695 14477696 14477697 14477698 14477699 14477700 14477701 14477702 14477703 14477704 14477705 14495537 14387081 14387087 14387088 14387089 14387090 14387091 14387093 14387094 14387095 14387098 14387099 14387100 14387101 14387102 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0814-2016%22
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