FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Newly Weds Foods, Inc.
- Product
- A20180 BATTER MIX X4 50.00 BAG
- Reason
- Products may contain Salmonella
- Published
- July 12, 2023
- Distribution
- ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Newly Weds Foods, Inc.
- Product
- S04380 BEEF RUB X1 50.00 BAG
- Reason
- Products may contain Salmonella
- Published
- July 12, 2023
- Distribution
- ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Newly Weds Foods, Inc.
- Product
- G96378 LOTTA ZING SAUCE MIX X2 15.00 CASE
- Reason
- Products may contain Salmonella
- Published
- July 12, 2023
- Distribution
- ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Newly Weds Foods, Inc.
- Product
- A89471 BATTER MIX X1 50.00 BAG
- Reason
- Products may contain Salmonella
- Published
- July 12, 2023
- Distribution
- ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Newly Weds Foods, Inc.
- Product
- A53643 BREADER X1 50.00 BAG
- Reason
- Products may contain Salmonella
- Published
- July 12, 2023
- Distribution
- ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Newly Weds Foods, Inc.
- Product
- A21470 BATTER MIX X1 50.00 BAG
- Reason
- Products may contain Salmonella
- Published
- July 12, 2023
- Distribution
- ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…
View recall →
FDA Recall
Terminated
Historical recordClass II
Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by Sun Pharmaceutical Medicare Limited, Baska Ujeti Road, Ujeti, Halol-389350, Gujarat, India, NDC 62756-0233-01
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Subpotent drug
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
StellaLife VEGA Oral Care Gel, 1 fl oz (30 ml) tubes, Peppermint, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-112-01
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
StellaLife VEGA Oral Care Gel, 1 fl oz (30 ml) tubes, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-102-02
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
StellaLife VEGA Oral Care Spray, 1 fl oz (30 ml) bottles, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-101-02
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
StellaLife VEGA Oral Care Rinse, 16 fl oz (473 ml) bottles, Coconut, Distributed by: StellaLife, Aventura, FL NDC 69685-113-16
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
StellaLife VEGA Oral Care Rinse, 16 fl oz (473 ml) bottles, Peppermint, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-103-16
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
SnoreStop Naso Spray Bulk, liquid, Distributed by Green Pharma, NDC 61152-199-99
by Homeocare Laboratories, Inc.
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical 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
View recall →
FDA Recall
Terminated
Historical 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
View recall →
FDA Recall
Terminated
Historical 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
View recall →
FDA Recall
Terminated
Historical 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
View recall →
FDA Recall
Terminated
Historical 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
View recall →
FDA Recall
Terminated
Historical 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
View recall →
FDA Recall
Terminated
Historical 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
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.
Read the full medical disclaimer.