Abbott Vascular recalls 20/30 INDEFLATORS with specific part numbers due to reported leaks and intermittent connections. Owners should check their device identifiers and lot numbers for affected units.
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Abbott Vascular is recalling 20/30 INDEFLATORS that have been reported to leak or have loose connections. This could lead to improper function of the device, though serious injury risks are not explicitly stated in the recall.
The device has been reported to leak or have intermittent/loose connections, which could cause improper function. However, the recall does not specify a risk of serious injury or death in normal use.
Users of the 20/30 INDEFLATOR device with specific part numbers and lot numbers listed in the recall are affected. Medical professionals using this device for procedures may be at higher risk due to potential device failure.
Check the device identifier (GTIN: 08717648013591) and lot numbers (60309678, 60320071, etc.) on your 20/30 INDEFLATOR. The product was sold starting March 1, 2019.
Identify your device's lot numbers and GTIN to confirm if it is affected by this recall.
The recall reports leaks and loose connections but does not specify a risk of serious injury or death in normal use.
Check your device's lot numbers and GTIN to see if it is affected; the recall does not include a remedy for affected units.
Look for the device identifier (GTIN: 08717648013591) and lot numbers (60309678, 60320071, etc.) on your 20/30 INDEFLATOR.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0921-2022 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0921-2022 from Abbott Vascular. 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.
