FDA Recall
🇺🇸 United States
TerminatedTerminated: December 15, 2022Historical recordClass II
Rebel Creamery
- Product
- Rebel Pistachio Ice Cream, one pint (473 mL, UPC 8 53149 008…
- Reason
- Pistachio ice cream may contain pistachio nut shells.
- Published
- May 4, 2022
- Distribution
- Multiple states
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FDA Recall
TerminatedTerminated: July 31, 2024Historical recordClass II
artnaturals Hand Sanitizer
by VIRGIN SCENT INC
- Reason
- CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: July 31, 2024Historical recordClass I
artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
by VIRGIN SCENT INC
- Reason
- Chemical Contamination: presence of benzene, acetaldehyde, and acetal.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
BPC-157 2 mg/mL (5 mL) Injection, 5 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: July 31, 2024Historical recordClass I
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.
by Pink Toyz
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: July 31, 2024Historical recordClass II
artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
by VIRGIN SCENT INC
- Reason
- CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
Sermorelin Acetate 1 mg/mL (6 mL) Injection, 6 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
PT-141 (Bremelanotide Acetate) 10 mg/mL (2 mL) Injection, 2mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
Melanotan II 1 mg/mL (10 mL) Injection, 10mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL (10 mL) Injection, 10 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 5, 2023Historical recordClass II
ARA-290 (Cibinetide Acetate) 6 mg/mL (4 mL) Injection, 4 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
by North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
- Reason
- Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: May 23, 2023Historical recordClass II
Rifampin for Injection, USP, 600 mg/vial, One Vial per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., NDC 67457-445-60
by MYLAN PHARMACEUTICALS INC
- Reason
- Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: October 25, 2023Historical recordClass II
Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred Pharmaceuticals, Inc., The Physicians Solutions, NDC 68788-7918-01
by Preferred Pharmaceuticals, Inc.
- Reason
- CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc. is discontinuing its stability study program.
- Published
- April 27, 2022
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordNot Yet Classified
Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
by Centric Compounding LLC
- Reason
- Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
- Published
- April 20, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: May 10, 2022Historical recordClass II
Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09
by Preferred Pharmaceuticals, Inc.
- Reason
- Out of specification results observed in dissolution during long term stability testing.
- Published
- April 20, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: June 27, 2024Historical recordClass III
Cyanocobalamin Injection, USP, 1,000 mcg per mL, For IM or SC Use Only, 1 mL Vial, Rx Only, Manufactured in India, for Auromedics Pharma LLC, NDC 55150-364-01.
by Aurobindo Pharma USA Inc.
- Reason
- Subpotent Drug: Out of Specification results for Assay
- Published
- April 20, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: June 20, 2023Historical recordClass I
IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use, 5mL Single Dose Vial, Rx Only, Teva Pharmaceuticals, USA, Inc., North Wales, PA 19454, NDC 0703-4154-11.
by Teva Pharmaceuticals USA Inc
- Reason
- Presence of Particulate Matter: Product was found to contain silica and iron oxide
- Published
- April 20, 2022
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 23, 2022Historical recordClass II
Bio-Botanica, Inc.
- Product
- NATURE's ANSWER Coral Calcium; Antioxidant Benefits*; 1000mg…
- Reason
- Product contained cesium chloride, a New Dietary Ingredient
- Published
- April 20, 2022
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: August 8, 2022Historical recordClass II
Skippy Foods, LLC.
- Product
- SKIPPY Creamy Peanut Butter Blended with Plant Protein NET W…
- Reason
- Potential to contain small steel contaminants.
- Published
- April 20, 2022
- Distribution
- CA, CT, DE, FL, HI, IL, IN, KS, MA, ME,…
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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