Stry: 3040-VenaFlow Calf Garment (Aircast) was mislabeled as 3010-PL Aircast Pos-Lock Connector. This could cause confusion with a different product intended for DVT prevention. Affected units have UDI: 00885825016661.
3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.
Stryker recalled 3040-VenaFlow Calf Garment units that were mislabeled as 3010-PL Aircast Pos-Lock Connectors. This confusion could lead users to think they have the wrong product, which might not be suitable for their medical needs.
The 3040-VenaFlow Calf Garment was incorrectly labeled as a 3010-PL Aircast Pos-Lock Connector. This could cause confusion about which product is intended for preventing deep vein thrombosis (DVT) and managing post-surgical recovery.
People who own or use the 3040-VenaFlow Calf Garment (Aircast) Quick Connect, especially those with medical conditions requiring compression sleeves. Those who have the mislabeled product may be at risk of using the wrong type of compression sleeve.
Check for the UDI code 00885825016661 on the product. The product was sold as a 3040-VenaFlow Calf Garment (Aircast) Quick Connect but mislabeled as 3010-PL Aircast Pos-Lock Connector.
Look for the UDI code 00885825016661 on the 3040-VenaFlow Calf Garment (Aircast) Quick Connect.
The 3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector.
Using the wrong product could lead to incorrect medical treatment, as the 3040-VenaFlow Calf Garment is intended for preventing deep vein thrombosis (DVT) and post-surgical recovery, while the 3010-PL is a different type of compression sleeve.
Check for the UDI code 00885825016661 on the product label. The product was sold as a 3040-VenaFlow Calf Garment but mislabeled as 3010-PL Aircast Pos-Lock Connector.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0272-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0272-2018 from Stryker. 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.
