FDA recall record

Retractable Technologies EasyPoint Needle, 25G x 5/8", REF: 82091 recall — FDA Z-1293-2024

The needle cannula of a retractable needle may detach from the needle holder in the patient.

Class IIclassification
Z-1293-2024official record ID
Mar 20, 2024report date

Recall record at a glance

Official recordZ-1293-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRetractable Technologies, Inc.
Report dateMar 20, 2024
Recall initiation dateFeb 5, 2024
Quantity477,600
LocationLittle Elm, TX, United States

Official product description

EasyPoint Needle, 25G x 5/8", REF: 82091

Why the product was recalled

The needle cannula of a retractable needle may detach from the needle holder in the patient.

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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