FDA recall record

Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile recall — FDA Z-2146-2023

Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.

Class IIclassification
Z-2146-2023official record ID
Jul 26, 2023report date

Recall record at a glance

Official recordZ-2146-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAesculap Implant Systems LLC
Report dateJul 26, 2023
Recall initiation dateMay 18, 2023
Quantity7 units
LocationCenter Valley, PA, United States

Official product description

Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610

Why the product was recalled

Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.

Distribution information

US Nationwide distribution in the states of DC, MO, PA, TX.

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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