AbbVie , Inc.
AbbVie , Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2015, with 4 FDA device recalls on record.
Top product codes for AbbVie , Inc.
FDA recalls by AbbVie , Inc.
- Z-2177-2017 — AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
- Z-2178-2017 — AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
- Z-2176-2017 — AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
- Z-0786-2017 — AbbVie PEG Kit 20 FR
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by AbbVie , Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.