EasyPoint Needle (Retractable) – Detachment Risk (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EasyPoint Needle, 25G x 5/8", REF: 82091
Brand
Retractable Technologies, Inc.
Lot Codes / Batch Numbers
UDI-DI: 00613703820907. Lot: K220402. Expiration: 03/28/2027
Products Sold
UDI-DI: 00613703820907. Lot: K220402. Expiration: 03/28/2027
Retractable Technologies, Inc. is recalling EasyPoint Needle, 25G x 5/8", REF: 82091 due to The needle cannula of a retractable needle may detach from the needle holder in the patient.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The needle cannula of a retractable needle may detach from the needle holder in the patient.
Recommended Action
Per FDA guidance
On 2/5/24, recall notices were sent to customers and distributors who were asked to do the following: 1) Segregate, quarantine, and discontinue use and distribution of affected devices. 2) Inform all personnel who have received or are receiving affected devices that they should not use affected devices. 3) If affected product was further distributed, notify these additional customers immediately. When notifying customers include a copy of the recall notice, label images, and the response form. 4) Complete and return the response form to rtiservice@retractable.com Customers with additional questions can email the firm at regulatory@retractable.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026