FDA recall record

Bard Peripheral Vascular Catalog # BEK4511, Qty: 10, Ecomomy Jamshidi Bone Marrow Biopsy and recall — FDA Z-0153-2022

Due to misbranded products shipped to customers.

Class IIclassification
Z-0153-2022official record ID
Oct 27, 2021report date

Recall record at a glance

Official recordZ-0153-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBard Peripheral Vascular Inc.
Report dateOct 27, 2021
Recall initiation dateAug 24, 2021
Quantity360 devices
LocationTempe, AZ, United States

Official product description

Catalog # BEK4511, Qty: 10, Ecomomy Jamshidi Bone Marrow Biopsy and Aspiration Tray, 11 G X 4"Biopsy/Aspiration needle, 15 G Aspiration Needle (Adjustable Length 15/16" -1-7/8") (24mm-48mm) sterile, For Single Use Only, RX only. Exp. Date Lidocaine Vendor lot. CareFusion. Original Jamshidi" Bone Marrow Biopsy/Aspiration Needle: - also referred to as Jamshidi needle Intended use for the posterior iliac crest biopsy technique

Why the product was recalled

Due to misbranded products shipped to customers.

Distribution information

U.S. Distribution: CA, GA,HI, IL, IN, LA, MO, MS, NC, OH, PA, PR, TX, UT, VA, and WA. OUS: None

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: E-Mail.

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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