AMEDA Purely Yours Breast Pump Recall: UK Power Adapter Issue
AMEDA recalls Purely Yours breast pumps (Model 17070PMW/17070ACA) with UK power adapters that may cause electrical issues. Affected units include Lot 7E058 and Lot 7E308.
Lower-risk recall
Two specific lots was incorrectly manufactured containing a UK power adapter.
Contact the company
What happened, in plain English
AMEDA is recalling two breast pumps (Model 17070PMW and 17070ACA) because specific lots had incorrectly manufactured UK power adapters. This could lead to electrical problems if the adapter is used with non-UK power sources. Read more at govinfonow.com/recall/73452-ameda-purely-yours-breast-pump-recall-uk-power-adapter-issue.
Source Summary by GovInfoNow · govinfonow.com/recall/73452-ameda-purely-yours-breast-pump-recall-uk-power-adapter-issue · Updated September 21, 2026 · FDA enforcement record: FDA #Z-0616-2018
Cite this page
“AMEDA Purely Yours Breast Pump Recall: UK Power Adapter Issue.” GovInfoNow, updated September 21, 2026. https://govinfonow.com/recall/73452-ameda-purely-yours-breast-pump-recall-uk-power-adapter-issue. Based on FDA recall #Z-0616-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0616-2018%22&limit=1).
Why it’s dangerous
The recalled lots contain UK power adapters that may not function properly with non-UK electrical systems. This could cause electrical malfunctions, but does not pose a direct risk of injury or damage under normal use conditions.
Who’s affected
Nursing mothers who own the specified breast pumps with Lot 7E058 or Lot 7E308 power adapters are affected. Those using the pumps with non-UK power sources may face electrical issues.
How to tell if you have this one
Check the pump model number (17070PMW or 17070ACA) and the lot number (7E058 or 7E308) on the packaging or label. The UK power adapter is included with these specific lots.
- Brand
AMEDA- Category
Medical device
What to do — step by step
Check Lot Number
Look for lot numbers 7E058 or 7E308 on the pump packaging or label.
Where it went and when
Where it was distributed
Distributed in 13 states and D.C..
FDA distribution: “Distributed to CA, DC, DE, FL, GA, IL, MD, NC, NJ, OH, TX, UT, VA, and WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Delaware, District of Columbia, Florida, Georgia, Illinois, Maryland, New Jersey, North Carolina, Ohio, Texas, Utah, Virginia, Washington.
Recall timeline
FDA published this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0616-2018 (July 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0616-2018 to see it in context.
- Plain-language summary written by qwen3:4b on September 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.