FDA Medical Device Recalls (openFDA)
Multi-Med, Inc.: 22ga x 1" Right Angle Huber Needle This product is a small gauge needle intended for single use hypodermic access to implanted ports.
- Recall number
- Z-1889-2010
- Recalling firm
- Multi-Med, Inc.
- Product
- 22ga x 1" Right Angle Huber Needle This product is a small gauge needle intended for single use hypodermic access to implanted ports.
- Status
- Terminated
- Initiated
- 2010-05-26
- Posted
- 2010-07-02
- Terminated
- 2017-05-23
- Reason
- FDA sample determined the needles to be coring.
- Root cause
- Pending
- Action
- The firm, Multi Med, Inc., sent an "URGENT: MEDICAL DEVICE RECALL" letter dated May 26, 2010 to their sole consignee Navilyst Medical, Inc., via email and overnight courier with signature notification. The letter describes the product, problem and action to be taken by customer. The customers was instructed to immediately examine their inventory and quarantine product subject to recall, if the product was distributed to others customers, identify and notify them at once and include recall notification letter,. Recall has been initiated due to FDAs sample analysis that these needles may core implanted port septums. If you have any questions, call me, Sue Starkey, at 603-357-8733 or via email at astarkey@multimedinc.com.
- Quantity
- 5,000
- Distribution
- Worldwide distribution
- Lot, serial or model codes
- Model number 10600219 Lot No 9B017M
- 510(k) numbers
- ["K891919"]
- PMA numbers
- not on file
- Product code
- FMI
- Firm FEI
- 1221765
- Firm city
- Keene
- Firm state
- NH
- 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