FDA Recall
OngoingHistorical recordClass II
BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, Applicator is sterile if package is intact, Flammable, External Use Only, 1 mL Applicator per pouch, 60 Applicators per inner carton, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., Made in the USA, Catalog Number 930480, NDC 54365-400-31.
by CareFusion 213, LLC
- Reason
- Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.
- Published
- May 28, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 8, 2025Historical recordClass I
My Life Inc
- Product
- Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg…
- Reason
- Undeclared milk allergen
- Published
- May 28, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.
by Empower Clinic Services, LLC dba Empower Pharmacy
- Reason
- Lack of Assurance of Sterility
- Published
- May 21, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube per Carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France.
by L'Oreal USA
- Reason
- cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
- Published
- May 21, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatment 0.7 fl. oz. (20 mL: UPC 883140035275) Tube, (benzoyl peroxide 0.5% and benzoyl peroxide 5.5% and salicylic acid 2%), La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France, UPC 883140035282 (kit).
by L'Oreal USA
- Reason
- cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
- Published
- May 21, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-Posay, France, UPC 883140500759.
by L'Oreal USA
- Reason
- Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.
- Published
- May 21, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: May 27, 2026Historical recordClass II
East CK Trading Inc.
- Product
- PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK…
- Reason
- Product contains undeclared sulfites (7.49mg/serving)
- Published
- May 21, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 23, 2026Historical recordClass II
Advance Food International Inc.
- Product
- National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.:…
- Reason
- Product contains elevated levels of lead (0.0649 mg/kg)
- Published
- May 21, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 3, 2025Historical recordClass I
Ray & Mascari,Inc
- Product
- Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam…
- Reason
- Potential Contamination of Salmonella.
- Published
- May 21, 2025
- Distribution
- IN KY MA MD MI NC OH PA WI
View recall →
FDA Recall
OngoingHistorical recordClass II
TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0121-01
by BSO LLC
- Reason
- Presence of Particulate Matter: Glass particles were found in pellet vials.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0122-01
by BSO LLC
- Reason
- Presence of Particulate Matter: Glass particles were found in pellet vials.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0124-01
by BSO LLC
- Reason
- Presence of Particulate Matter: Glass particles were found in pellet vials.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0125-01
by BSO LLC
- Reason
- Presence of Particulate Matter: Glass particles were found in pellet vials.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0101-01
by BSO LLC
- Reason
- Presence of Particulate Matter: Glass particles were found in pellet vials.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
temper tamer, 1 US fl oz. (29.6 mL), Homeopathic Oral Spray, Manufactured by: Siddha Flower Essences, Oxnard, CA, 93030 NDC 69779-020-01.
by Siddha Flower Essences, LLC.
- Reason
- CGMP Deviations
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Polyvinyl Alcohol Ophthalmic Solution 1.4%, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-678-15.
by BRS Analytical Services, LLC
- Reason
- cGMP deviations and lack of assurance of sterility.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Lubricant Eye Drops Solution, Polyethylene Glycol 400 0.4% Eye Lubricant, Propylene Glycol 0.3% Eye Lubricant, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-126-15.
by BRS Analytical Services, LLC
- Reason
- cGMP deviations and lack of assurance of sterility.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Carboxymethlycellulose Sodium 0.5% Eye Lubricant, Lubricating Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-068-15.
by BRS Analytical Services, LLC
- Reason
- cGMP deviations and lack of assurance of sterility.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Carboxymethylcellulose Sodium Ophthalmic Gel 1%, Carboxymethlycellulose Sodium 1% Eye Lubricant, Lubricant Eye Gel, Soothing Gel, Sterile, 0.5 FL OZ (15mL) per bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-066-15.
by BRS Analytical Services, LLC
- Reason
- cGMP deviations and lack of assurance of sterility.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Artificial Tears Ophthalmic Solution, Dextran 70.01%/Glycerin 0.2%/Hypromellose 0.3% (Eye Lubricants) Lubricant Eye Drops, STERILE, 0.5 FL OZ (15 mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-043-15.
by BRS Analytical Services, LLC
- Reason
- cGMP deviations and lack of assurance of sterility.
- Published
- May 14, 2025
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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