FDA Recall
TerminatedTerminated: September 16, 2024Historical recordClass II
DoloEar Earache Drops, 0.50 fl. oz. bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-001-15
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: September 16, 2024Historical recordClass II
Babelyn Diarrhea Drops Homeopathic Remedy, 0.5 fl. oz. (15 mL) bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-035-01
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: September 16, 2024Historical recordClass II
Bebelyn Colic Drops Homeopathic Remedy, 0.5 FL Oz (15 mL) bottles, distributed by Pharmadel LLC Georgetown, DE NDC 55758-036-01
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: September 16, 2024Historical recordClass II
Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: September 16, 2024Historical recordClass II
Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured For: Acutens, Inc., Sheridan, WY NDC 80551-201-02
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: August 5, 2024Historical recordClass II
Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 vaginal inserts with 21 disposable vaginal applicators, Manufactured for: Ferring Pharmaceuticals Inc., Parsippany, NJ NDC# 55566-6500-03
by Ferring Pharmaceuticals Inc
- Reason
- cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: April 30, 2024Historical recordClass II
Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count Tablets Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-7179-61
by The Harvard Drug Group
- Reason
- Packaging defect: blister packaging inadequately sealed.
- Published
- July 5, 2023
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: November 21, 2024Historical recordClass II
MOTTS LLP
- Product
- Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Contai…
- Reason
- Elevated patulin levels
- Published
- July 5, 2023
- Distribution
- US states including: AL, CT, FL, GA, IA…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: October 4, 2023Historical recordClass III
Anatox Inc
- Product
- Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber…
- Reason
- Elevated lead levels
- Published
- July 5, 2023
- Distribution
- Distributors, retailers, and consumers i…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: October 4, 2023Historical recordClass III
Anatox Inc
- Product
- 1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an ambe…
- Reason
- Elevated lead levels
- Published
- July 5, 2023
- Distribution
- Distributors, retailers, and consumers i…
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FDA Recall
TerminatedTerminated: July 2, 2024Historical recordClass I
ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited Bachupally-500 090 India, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-6269-08
by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
- Reason
- Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.
- Published
- June 28, 2023
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: August 28, 2024Historical recordClass III
Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01
by Aurolife Pharma, LLC
- Reason
- Failed Impurities/Degradation Specifications
- Published
- June 28, 2023
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 14, 2024Historical recordClass II
Julian's Recipe, LLC
- Product
- Julian's Recipe CAULI-WAFEL SANDWICHES TURKEY SAUSAGE & CH…
- Reason
- Contains undeclared soy lecithin
- Published
- June 28, 2023
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 14, 2024Historical recordClass II
Julian's Recipe, LLC
- Product
- Julian's Recipe Maple & Brown Butter Cauli-Wafels, 7.41 oz.
- Reason
- Contains undeclared soy lecithin
- Published
- June 28, 2023
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 14, 2024Historical recordClass II
Julian's Recipe, LLC
- Product
- Julian's Recipe Original Cauli-Wafels, 7.41 oz.
- Reason
- Contains undeclared soy lecithin
- Published
- June 28, 2023
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: March 22, 2024Historical recordClass II
ENTRINSIC HEALTH SOLUTION INC
- Product
- enterade Advanced Oncology Formula; Original Vanilla Flavor;…
- Reason
- Potential for the product to develop mold and spoil.
- Published
- June 28, 2023
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 7, 2025Historical recordClass I
Aquamar Inc
- Product
- Kanimi Crab Flavored Seafood Fancy Shred Style 92410 Ingredi…
- Reason
- Product found to contain undeclared wheat and eggs
- Published
- June 28, 2023
- Distribution
- U.S. distribution to the following: AZ,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 7, 2025Historical recordClass I
Aquamar Inc
- Product
- Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM…
- Reason
- Product found to contain undeclared wheat and eggs
- Published
- June 28, 2023
- Distribution
- U.S. distribution to the following: AZ,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 7, 2025Historical recordClass I
Aquamar Inc
- Product
- Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ing…
- Reason
- Product found to contain undeclared wheat and eggs
- Published
- June 28, 2023
- Distribution
- U.S. distribution to the following: AZ,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 17, 2024Historical recordClass II
Nutricia North America
- Product
- TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g)…
- Reason
- Infant formula contains undeclared tyrosine
- Published
- June 28, 2023
- Distribution
- Alaska, California, Connecticut, Florida…
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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