RecallWatchUSA

Home / Brands / DermaRite Industries

DermaRite Industries Recalls

22 recalls on record · September 10, 2025 to November 26, 2025 · Drugs

November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Berg
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), a
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenu
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West S
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distribu
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 619
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls 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-
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) p
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), an
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls 4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
September 10, 2025DrugsFDA
DermaRite Industries, LLC recalls PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777
Hazard: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
September 10, 2025DrugsFDA
DermaRite Industries, LLC recalls KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Indu
Hazard: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
September 10, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Sid
Hazard: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
September 10, 2025DrugsFDA
DermaRite Industries, LLC recalls DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.) b
Hazard: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
DermaRite Industries Recalls | RecallWatchUSA