Linet recalls AVE 2 Birthing Beds with incorrect manufacturer label on device. These beds are for vaginal delivery use only, not general hospital beds. Affected units have specific model and lot numbers.
The UDI on the device label indicates incorrect manufacturer.
Linet is recalling AVE 2 Birthing Beds that have an incorrect manufacturer label on the device. These beds are designed only for vaginal delivery use and not for general hospital beds. The recall is due to a labeling error that could cause confusion about who made the product.
The device label shows the wrong manufacturer name. This could lead to confusion about the product's origin, but the bed itself is designed for vaginal delivery use only and not for general hospital beds. The labeling error does not pose a direct safety risk to users.
Mothers using the AVE 2 Birthing Bed for vaginal delivery are likely affected. Healthcare providers who use these beds for delivery purposes are at risk of confusion due to the incorrect label.
Check for model numbers 4BCPPB-3XCZ0002 (lot numbers PPB1155 to PPB1284, etc.) or 4BCPPB-CCZ0008 (lot PPB1446 to PPB1449) or 4BCPPB-BCZ0009 (lot PPB1541 to PPB1542). The bed is intended for vaginal delivery use only, not general hospital beds.
Look for the model number and lot numbers on the device label to confirm if it is affected.
The recall is due to an incorrect manufacturer label on the device, which could cause confusion about the product's origin.
Yes, the bed is designed for vaginal delivery use only and not for general hospital beds. The labeling error does not affect safety.
Check the model number and lot numbers on the device label to see if it is affected. If it is, contact Linet for more information.
We’ve drafted a message you can send Linet to request your refund or repair — edit it as you like.
Subject: Recall Z-2781-2020 — Linet Linet Hello, I own a Linet that is covered by recall Z-2781-2020 from Linet. 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.
