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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77526

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

Open FDA event record

Event summary

Timeline bucket
June 08, 2017
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Phillips Co.

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

6 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 6

Tetracycline-ABC Brand Topical ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 4307410201

D-0947-2017
Recall number
D-0947-2017
Initiated
June 08, 2017
Classification
Class II
Status
Terminated
Recalling firm
Phillips Co.
Quantity
100-200 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
GMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide and United Kingdom

drug · product 2 of 6

TetraStem brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-301-11

D-0948-2017
Recall number
D-0948-2017
Initiated
June 08, 2017
Classification
Class II
Status
Terminated
Recalling firm
Phillips Co.
Quantity
200-300 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
GMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide and United Kingdom

drug · product 3 of 6

Diabecline brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-100-11

D-0949-2017
Recall number
D-0949-2017
Initiated
June 08, 2017
Classification
Class II
Status
Terminated
Recalling firm
Phillips Co.
Quantity
100-200 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
GMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide and United Kingdom

drug · product 4 of 6

StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 04307-100-11

D-0950-2017
Recall number
D-0950-2017
Initiated
June 08, 2017
Classification
Class II
Status
Terminated
Recalling firm
Phillips Co.
Quantity
20-50 bottles/units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
GMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide and United Kingdom

drug · product 5 of 6

StaphWash+Plus+ Skin Protectant, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 43074-101-01

D-0951-2017
Recall number
D-0951-2017
Initiated
June 08, 2017
Classification
Class II
Status
Terminated
Recalling firm
Phillips Co.
Quantity
10-30 bottles/units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
GMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide and United Kingdom

drug · product 6 of 6

VenomX, Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottles, Skin Protectant Phillips Company, Millerton, OK -- NDC 43074-207-01

D-0952-2017
Recall number
D-0952-2017
Initiated
June 08, 2017
Classification
Class II
Status
Terminated
Recalling firm
Phillips Co.
Quantity
20-50 bottles/units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
GMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured by the firm.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide and United Kingdom