Medela Breast Milk Transfer Lid Recall: Packaging May Be Compromised
Medela recalls breast milk transfer lids (model 90003S-100) due to potential packaging breaches that could compromise sterility. Affected units have specific lot codes.
Lower-risk recall
The sterility may be compromised due to a potential breach in the packaging, even though it may appear intact.
Contact the company
What happened, in plain English
Medela is recalling breast milk transfer lids for oral syringe connectors because the packaging might be breached, risking contamination. This could lead to infections if the lids are used without proper sterility. Read more at govinfonow.com/recall/69383-medela-breast-milk-transfer-lid-recall-packaging-may-be-compromised.
Source Summary by GovInfoNow · govinfonow.com/recall/69383-medela-breast-milk-transfer-lid-recall-packaging-may-be-compromised · Updated August 20, 2026 · FDA enforcement record: FDA #Z-2061-2019
Cite this page
“Medela Breast Milk Transfer Lid Recall: Packaging May Be Compromised.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69383-medela-breast-milk-transfer-lid-recall-packaging-may-be-compromised. Based on FDA recall #Z-2061-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2061-2019%22&limit=1).
Why it’s dangerous
The packaging might have a breach that isn't visible, which could compromise the sterility of the lid. This means the lid might not be clean enough for safe use with breast milk.
Who’s affected
Babies and caregivers using Medela breast milk transfer lids with oral syringe connectors. Those with specific lot codes are most at risk.
How to tell if you have this one
Check for lot codes: 441113, 441825, 441965, 442099, 442188, 442494, 442612, 443265, 443557, 444054, 444317, 445260, 445310, 445470, 445678, 446402, 446518, 446916, 447447, 447470, 447789. The product is model 90003S-100.
- Brand
Medela- Category
Medical device
What to do — step by step
Check Lot Codes
Look for lot codes on the product: 441113, 441825, 441965, 442099, 442188, 442494, 442612, 443265, 443557, 444054, 444317, 445260, 445310, 445470, 445678, 446402, 446518, 446916, 447447, 447470, 447789.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 8 states.
FDA distribution: “Nationwide distribution in IL, MO, NE, OH, RI, TN, TX, VA. International distribution in Canada Internal Medela and sales reps located in CA, CO, IL, LA, NC, NJ, NV, PA, SC, TN, TX Domestic Hospitals located in AL, AR, AZ, CA, CO, CT, DE,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Illinois, Missouri, Nebraska, Ohio, Rhode Island, Tennessee, Texas, Virginia.
Recall timeline
FDA terminated this recall 21 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-2061-2019 (December 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2061-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 20, 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.