FDA recall record

AbbVie PEG Kit 20 FR recall — FDA Z-0786-2017

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…

Class IIclassification
Z-0786-2017official record ID
Dec 28, 2016report date

Recall record at a glance

Official recordZ-0786-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAbbVie Inc.
Report dateDec 28, 2016
Recall initiation dateNov 22, 2016
Quantity541 units
LocationNorth Chicago, IL, United States

Official product description

AbbVie PEG Kit 20 FR

Why the product was recalled

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.

Distribution information

U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.

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: Letter.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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