FDA Medical Device Recalls (openFDA)
AbbVie Inc.: AbbVie PEG Kit 20 FR
- Recall number
- Z-0786-2017
- Recalling firm
- AbbVie Inc.
- Product
- AbbVie PEG Kit 20 FR
- Status
- Terminated
- Initiated
- 2016-11-22
- Posted
- not on file
- Terminated
- 2019-07-09
- Reason
- AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.
- Root cause
- Device Design
- Action
- The firm sent an URGENT: MEDICAL DEVICE FIELD CORRECTION NOTIFICATION AbbVie PEG Kit 20 FR to affected customers describing the reason for the notification. The letter asks affected customers to forward this letter to all Movement Disorder Specialists and physicians (e.g. GIs, IRs, and surgeons) that place PEG- J Tubes within your facility. The letter describes actions to be taken for patients still using the AbbVie PEG 20FR Tube. The letter requests user facilities to continue to monitor the performance of the Tube. The firm states that there is no need to replace the AbbVie PEG 20FR Tube if it is functioning as expected and maintaining a viable connection with the Y-Connector. The letter provides the following instructions when establishing a connection between Abbvie PEG 20FR Tube with the 20FR Y-connector, always refer to AbbVie J Intestinal Tube 9 FR to PEG 15 and 20 FR Instructions for Use for 62918-001. The letter notes the following: 1. Ensure that the set-up process clearly follows the sequence of events as described in the instructions for use and the following clarifications. 2. Ensure that the AbbVie PEG 20FR tube is connected to the corresponding 20 Y- connector (see photograph below which shows the difference between the 15FR and 20FR connection diameter). 3. DO NOT USE ALCOHOL CONTAINING PRODUCTS with the AbbVie PEG 20 FR tube as this may result in damage to the tube. 4. Ensure that the Tube Clamp and Tube Clip on Fixation Plate are both closed. 5. Cut off the proximal cone and Fixation Loop of the AbbVie PEG Tube (15FR or 20FR). Note: Ensure that the cut is perpendicular (90 degree angle) to the tube and not on a diagonal as this ensures proper seating of the tube when engaged into the pin of the Y-connector fitting. 6. Slide the colored Fixation Screw (including the outer ring) over the Abbvie PEG Tube: a. For 15 FR, use the Blue/White screw b. For 20 FR, use the Violet/White screw 7. Grasp near the
- Quantity
- 541 units
- Distribution
- U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.
- Lot, serial or model codes
- AbbVie PEG Kit 20 Fr Product Code 62912-01-16 with lot numbers: 32025245, 32265215, 32335206, 32335336
- 510(k) numbers
- K142793
- PMA numbers
- not on file
- Product code
- KNT
- Firm FEI
- 3009751352
- Firm city
- North Chicago
- Firm state
- IL
- 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