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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97625

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

Open FDA event record

Event summary

Timeline bucket
August 27, 2025
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
DermaRite Industries, LLC

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

18 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 18

4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04

D-0160-2026
Recall number
D-0160-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
3,178 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027.

Distribution pattern

Nationwide in the USA

drug · product 2 of 18

DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174-04) and b) 454 g (16 oz.) per jar (NDC 61924-174-16), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0161-2026
Recall number
D-0161-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
Unavailable

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 3 of 18

DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0162-2026
Recall number
D-0162-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
1,480 packets

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 4 of 18

DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) per tube (NDC 61924-092-08), b) 800 mL (27 fl. oz.) per bag (NDC 61924-092-27), and c 1000 mL (34 fl. oz.) per bag (NDC 61924-092-34), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0163-2026
Recall number
D-0163-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
7,736 tubes

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 5 of 18

DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04

D-0164-2026
Recall number
D-0164-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
2,673 tubes

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 6 of 18

DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08

D-0165-2026
Recall number
D-0165-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
2,389 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 7 of 18

GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and c) 800 mL (NDC 61924-106-27), and d) 1000 mL (NDC 61924-106-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0166-2026
Recall number
D-0166-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
115,994 containers

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 8 of 18

Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0167-2026
Recall number
D-0167-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
576 containers

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 9 of 18

KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34

D-0168-2026
Recall number
D-0168-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
15,267 cartridges

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 10 of 18

Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0169-2026
Recall number
D-0169-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
8,378 containers

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 11 of 18

Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0170-2026
Recall number
D-0170-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
57,837 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 12 of 18

McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distributed by McKesson Medical-Surgical Inc., Richmond, VA 23233.

D-0171-2026
Recall number
D-0171-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
5,876 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 13 of 18

PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08

D-0172-2026
Recall number
D-0172-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
16,006 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 14 of 18

PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0173-2026
Recall number
D-0173-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
381,619 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 15 of 18

Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04

D-0174-2026
Recall number
D-0174-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
37,272 tubes

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 16 of 18

Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), and c) 800 mL (NDC 61924-405-27), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0175-2026
Recall number
D-0175-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
57,041 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 17 of 18

San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34

D-0176-2026
Recall number
D-0176-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
15,465 cartridges

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA

drug · product 18 of 18

UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04

D-0177-2026
Recall number
D-0177-2026
Initiated
August 27, 2025
Classification
Class II
Status
Ongoing
Recalling firm
DermaRite Industries, LLC
Quantity
37,379 spray bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information

All lots on or before expiry date 08/2027

Distribution pattern

Nationwide in the USA