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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85848

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

Open FDA event record

Event summary

Timeline bucket
June 16, 2020
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Glaxosmithkline Consumer Healthcare Holdings

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

Complete imported group

Every recalled product in this event

2 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 2

Childrens Robitussin Honey Cough and Chest Congestion DM, dextromethorphan (cough suppressant), guaifenesin (expectorant), 4 FL OZ. bottle (118 mL), Distributed by: Pfizer, Madison, NJ 07940 USA, UPC: 50300318760128, NDC: 0031-8760-12.

D-1361-2020
Recall number
D-1361-2020
Initiated
June 16, 2020
Classification
Class II
Status
Terminated
Quantity
132,336 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Code information

Lot #s: 02177, 02178, Exp. 01/31/2022

Distribution pattern

Nationwide in the US

drug · product 2 of 2

Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ 07940, Made in Canada, UPC: 60300312234196, NDC: 0031-2234-19.

D-1362-2020
Recall number
D-1362-2020
Initiated
June 16, 2020
Classification
Class II
Status
Terminated
Quantity
78,132 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Code information

Lot CL8292, Exp. 09/30/2021

Distribution pattern

Nationwide in the US