Westmed recalls adult oxygen masks with potential loose connections that could delay treatment. Affected models include REF 3102-E with 8' tubing. Consumers should check product details and contact Westmed for remedies.
There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Westmed is recalling adult oxygen masks that may have loose connections between the oxygen tube and mask adapter. This could delay critical treatment for patients needing oxygen therapy.
The oxygen delivery tube might become loose when connecting to the mask adapter. This could cause a delay in oxygen delivery during critical medical situations, potentially worsening a patient's condition.
Patients using medical oxygen therapy with this mask model are affected. Those with respiratory conditions requiring continuous oxygen delivery are at higher risk.
Check for the model REF 3102-E with 8-foot tubing. The product was sold with lot number 091120N53. This mask requires a prescription (Rx Only).
Look for the model number REF 3102-E and lot number 091120N53 on the mask packaging.
Reach out to Westmed directly for instructions on how to fix or replace the mask.
The recall indicates a potential risk of loose connections that could delay treatment, so it is not recommended for use until fixed.
Check for the model REF 3102-E with 8-foot tubing and lot number 091120N53 on the packaging.
Contact Westmed directly for instructions on how to fix or replace the mask.
We’ve drafted a message you can send Westmed to request your refund or repair — edit it as you like.
Subject: Recall Z-0741-2021 — Westmed Westmed Hello, I own a Westmed that is covered by recall Z-0741-2021 from Westmed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
