EasyPoint Needle recall
EasyPoint Needle, 25G x 5/8", REF: 82091
Why was EasyPoint Needle recalled?
The needle cannula of a retractable needle may detach from the needle holder in the patient.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 00613703820907. Lot: K220402. Expiration: 03/28/2027
- Product
- EasyPoint Needle, 25G x 5/8", REF: 82091
- Recalling firm
- Retractable Technologies, Inc.
- Quantity
- 477,600
- Distribution
- US Nationwide distribution including in the states of NY, FL, IL, MA, UT, NJ, AZ, MO, WA, NC, CA, TX, NV, IN, PA, VA, IA, GA, TN, MI, OH, OK, CO, OR, SC, MN, CT.
- Recall date
- March 20, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)