FDA Recall
🇺🇸 United States
TerminatedTerminated: March 6, 2026Historical recordClass II
Dollar General Corporation
- Product
- Clover Valley 1% Low Fat Chocolate Milk, 1/2 GAL (1.89 L), p…
- Reason
- Temperature abuse due to temperature excursion in one shipping trailer
- Published
- August 13, 2025
- Distribution
- LA
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 6, 2026Historical recordClass II
Dollar General Corporation
- Product
- Clover Valley One Dozen Grade A Eggs Large, 12 ct, packaged…
- Reason
- Temperature abuse due to temperature excursion in one shipping trailer
- Published
- August 13, 2025
- Distribution
- LA
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 6, 2026Historical recordClass II
Dollar General Corporation
- Product
- Clover Valley Shredded Parmesan Cheese, NET WT 6 OZ (170g),…
- Reason
- Temperature abuse due to temperature excursion in one shipping trailer
- Published
- August 13, 2025
- Distribution
- LA
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 6, 2026Historical recordClass II
Dollar General Corporation
- Product
- Chobani Vanilla Greek Yogurt, 4 OZ (113g), packaged in a pla…
- Reason
- Temperature abuse due to temperature excursion in one shipping trailer
- Published
- August 13, 2025
- Distribution
- LA
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 6, 2026Historical recordClass II
Dollar General Corporation
- Product
- Chobani Flip Cookie Dough Greek Yogurt, NET WT. 4.5 OZ (128g…
- Reason
- Temperature abuse due to temperature excursion in one shipping trailer
- Published
- August 13, 2025
- Distribution
- LA
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 6, 2026Historical recordClass II
Dollar General Corporation
- Product
- Checkers Famous Seasoned Fries, NET WT 28 OZ (1 LB 12 OZ) 79…
- Reason
- Temperature abuse due to temperature excursion in one shipping trailer
- Published
- August 13, 2025
- Distribution
- LA
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FDA Recall
🇺🇸 United States
OngoingHistorical recordClass I
Doehler North America, Inc.
- Product
- Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.3…
- Reason
- Listeria monocytogenes. During routine testing the firm received positive test results for Listeria monocytogenes.
- Published
- August 13, 2025
- Distribution
- Product was shipped to the following: Di…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 13, 2026Historical recordClass II
QUEEN BEE GARDENS
- Product
- Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Inte…
- Reason
- Product may have small flakes of stainless steel in product.
- Published
- August 13, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 13, 2026Historical recordClass II
QUEEN BEE GARDENS
- Product
- Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended u…
- Reason
- Product may have small flakes of stainless steel in product.
- Published
- August 13, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 13, 2026Historical recordClass II
QUEEN BEE GARDENS
- Product
- Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Inte…
- Reason
- Product may have small flakes of stainless steel in product.
- Published
- August 13, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton, Rx Only, Manufactured by: Hikma Berkeley Heights, NJ 07922, NDC# 0641-6044-25
by Hikma Pharmaceuticals USA Inc.
- Reason
- Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
- Published
- August 6, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Sucralfate Tablets, USP 1 gram, packaged in a) 100-count bottles NDC 29033-0003-01, and b) 500-count bottles, NDC 29033-0003-05), Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120.
by Nostrum Laboratories, Inc.
- Reason
- CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
- Published
- August 6, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Cinacalcet Tablets 90 mg, 30-count bottles, Rx only, Manufactured by: Strides Pharma Science Ltd. Puducherry, India; Distributed by: Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-885-04
by Strides Pharma, Inc.
- Reason
- Failed Dissolution Specifications.
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04
by Pfizer Inc.
- Reason
- CGMP Deviations; particulates identified during visual inspection
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10, Syringe NDC - 60793-701-02
by Pfizer Inc.
- Reason
- CGMP Deviations; particulates identified during visual inspection
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05.
by FDC Limited
- Reason
- Defective Container: spike of the cap becomes lodged in the nozzle of the product bottle.
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
CompletedHistorical recordClass II
Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL, 34108, United States, Manufactured by: Lupin Limited, Goa 103 722, INDIA, NDC 68180-755-01.
by Lupin Pharmaceuticals Inc.
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 21, 2025Historical recordClass II
NuNaturals Inc
- Product
- Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187…
- Reason
- Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener.
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 21, 2025Historical recordClass II
NuNaturals Inc
- Product
- Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Produ…
- Reason
- Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
- Published
- August 6, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton)
by Cipla USA, Inc.
- Reason
- Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
- Published
- July 30, 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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