FDA Device recall Z-3071-2017
CADD(R) Medication Cassette Reservoir with clamp and female Luer
- FDA Device
- Class II
- terminated
- Published 2017-09-06
On 2017-09-06 the FDA classified a Class II recall of CADD(R) Medication Cassette Reservoir with clamp and female Luer by Smiths Medical Asd, citing the medication cassette reservoir, part number 21-7002-24, with lot number 16X659, may have been manufactured with the incorrect pressure plate and the tubing used on the cassette….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3071-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-05 |
| Published | 2017-09-06 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Smiths Medical Asd |
| Distribution | n/a |
Product
CADD(R) Medication Cassette Reservoir with clamp and female Luer. Non vented stopper included, REF 21-7002-24, Rx only, STERILE EO, Manufacturer Smiths Medical ASD, Inc.
Reason
The medication cassette reservoir, part number 21-7002-24, with lot number 16X659, may have been manufactured with the incorrect pressure plate and the tubing used on the cassette may have been routed incorrectly.
Identifiers
| code_info | lot number 16X659 |
|---|
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-3071-2017%22
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