Recall events
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Event 91259
Event summary
Timeline bucket December 06, 2022
Product types Drug
Classifications Class I
Statuses Terminated
Recalling firm wording Glaxosmithkline Consumer Healthcare Holdings DBA Haleon
Dossier provenance
Source snapshots represented here
openFDA Drug 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.
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
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
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.
drug · product 1 of 3
Advil (ibuprofen) Tablets, 200 mg, packaged as a) 360-count bottles (UPC 3 0573 0154 60 4), and b) 200-count bottles (UPC 3 0573 0154 21 5), Pfizer, Madison, NJ 07940
D-0181-2023
Recall number D-0181-2023
Initiated December 06, 2022
Classification Class I
Status Terminated
Quantity 321,246 tablets
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
Code information a) Lots EJ2218, EJ2219, EJ2220, Exp 09/2023; b) Lot 953D, Exp 05/2025
Distribution pattern Nationwide in the USA.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12572]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 3
Advil Liqui Gels, Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Distributed by: Pfizer, Madison, NJ 07940, UPC 3 0573 0169 49 3
D-0182-2023
Recall number D-0182-2023
Initiated December 06, 2022
Classification Class I
Status Terminated
Quantity 88,380 capsules
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
Code information Lot: R94065, Exp 02/29/2024
Distribution pattern Nationwide in the USA.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12775]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 3
Advil Liqui Gels (minis), Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID), 200 liquid filled capsules, Pfizer, Madison, NJ 07940, UPC 3 0573 1769 13 5
D-0183-2023
Recall number D-0183-2023
Initiated December 06, 2022
Classification Class I
Status Terminated
Quantity 209,292 capsules
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
Code information Lot: R93517, R94072, R94073, Exp 02/29/2024; T00655, Exp 03/31/2025
Distribution pattern Nationwide in the USA.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[12704]
FDA event record
· Exact recall-number query on openFDA
