FDA Device recall Z-0616-2018
Purely Yours Breast Pump
- FDA Device
- Class III
- ongoing
- Published 2018-02-21
On 2018-02-21 the FDA classified a Class III recall of Purely Yours Breast Pump by Ameda, citing two specific lots was incorrectly manufactured containing a UK power adapter.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0616-2018 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2017-07-10 |
| Published | 2018-02-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ameda |
| Distribution | CA, DC, DE, FL, GA, IL, MD, NC, NJ, OH, TX, UT, VA, WA |
Product
Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended to express and collect the mother s milk from the breasts of a nursing woman for the purpose of feeding the collected milk to a baby.
Reason
Two specific lots was incorrectly manufactured containing a UK power adapter.
Identifiers
| code_info | Lot 7E058 and Lot 7E308 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0616-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.