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FDA Medical Device Recalls (openFDA)

Becton Dickinson & Company: BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications

Recall number
Z-1009-2012
Recalling firm
Becton Dickinson & Company
Product
BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications
Status
Terminated
Initiated
2011-10-08
Posted
2012-02-13
Terminated
2012-12-11
Reason
Becton Dickinson has identified clogged needles.
Root cause
Device Design
Action
Becton Dickinson sent Urgent Product Recall letters dated October 18, 2011 and October 17, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory to deterine if they have any of the affected product. If they have affected product customers should return the product to Beckton Dickinson. For any questions regarding this recall call 201-847-4344.
Quantity
480,000 units
Distribution
Nationwide Distribution including IL and NJ
Lot, serial or model codes
Marketing Status: K021475 Device Listing Number: DQ41418 Reorder#300745, Lot#lll6090
510(k) numbers
["K021475"]
PMA numbers
not on file
Product code
FMI
Firm FEI
2243072
Firm city
Franklin Lakes
Firm state
NJ
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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