Exact FDA event identifier

Event 77129

3 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: April 27, 2017
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: AbbVie Inc.

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

Z-2176-2017

Recall number: Z-2176-2017
Initiated: April 27, 2017
Classification: Class II
Status: Terminated
Recalling firm: AbbVie Inc.
Quantity: 673 kits

App-derived interpretation

No assignment exists because the official recall reason is blank.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Unavailable

Code information

Material/List number: 629100116 Lots: 32025245, 32054247, 32265215, 32335206, 32335336

Distribution pattern

Nationwide, Albania, Austria, Australia, Belgium, Bulgaria, Canada, Switzerland, Czech Republic, Germany, Denmark, Estonia, Spain, Finland, France, Great Britain, Greece, Croatia, Hungary, Ireland, Italy, Japan, Korea, Luxembourg, Netherlands, Norway, Portugal, Romania, Russia, Saudi Arabia, Sweden, Slovenia, Slovakia, Turkey

device · product 2 of 3

AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

Z-2177-2017

Recall number: Z-2177-2017
Initiated: April 27, 2017
Classification: Class II
Status: Terminated
Recalling firm: AbbVie Inc.
Quantity: Unavailable

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

missing label

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

PEG kits have the potential for one of the following defects: missing components, duplicate components or missing label/Instructions for Use, which includes expiry information.

Code information

Material/List number: 629100116 Lots: 32025235, 32184275, 32354106, 32365305, 32435265

Distribution pattern

device · product 3 of 3

AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

Z-2178-2017

Recall number: Z-2178-2017
Initiated: April 27, 2017
Classification: Class II
Status: Terminated
Recalling firm: AbbVie Inc.
Quantity: 3,331 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

missing label

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

PEG kits have the potential for one of the following defects: missing components, duplicate components or missing label/Instructions for Use, which includes expiry information.

Code information

Material/List number: 62918001 Lots: 32044225, 32155205, 32344326, 32461215