FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Domino Foods Inc
- Product
- 50# (pound) Domino Light Brown Sugar. This is packaged in b…
- Reason
- Syrup used to manufacture Light Brown Sugar may have been exposed to extraneous material, specifically a bird.
- Published
- July 13, 2022
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Prairie City Bakery
- Product
- Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey…
- Reason
- Salmonella. Product contains recalled Jif peanut butter as ingredient.
- Published
- July 13, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 29765500000 Cupcake 6 Buckeye 18Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 25136000000 Bakery, Cake, Chocolate, Peanut Butter Iced 8…
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 25135900000 Bakery, Brownie, Peanut Butter Creme 16Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 25115700000 Bakery, Cake, Peanut Butter Fudge Split 25.6…
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 25022900000 Peanut Butter Fudge Bar Cake 22.6 Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 24777800000 Brownie Classic Peanut Bttr 8c , 14Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 23984200000 Torte Peanut Butter 62Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 22985000000 Petite Cake Peanut Butter 18Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE 22777900000 Brownie Tray Classic - 24 Ct., 24Oz
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE Bakery, Gob, Mini, Chocolate, Peanut Butter Icing
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Giant Eagle
- Product
- GE Bakery, Cookie, Thumbprint, Peanut Butter, 12 Oz., Clam S…
- Reason
- Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
- Published
- July 13, 2022
- Distribution
- The product was distributed domestically…
View recall →
FDA Recall
Terminated
Historical recordClass II
Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16
by Akorn, Inc.
- Reason
- Defective container: defect prevents product from dispensing as intended.
- Published
- July 6, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02
by Akorn, Inc.
- Reason
- Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.
- Published
- July 6, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186 By Noven Pharmaceuticals, Inc., Miami, FL 33186. NDC 68968-5552-3
by Noven Pharmaceuticals Inc
- Reason
- Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
- Published
- July 6, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass I
SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc. Camarillo, CA 93012, NDC 61152-199-99, UPC 7 69682 29101 3
by Green Pharmaceuticals, Inc.
- Reason
- Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.
- Published
- July 6, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC # 33342-052-44, Rx Only, MFR: Macleods Pharma USA, Inc. Plainsboro, NJ 08536
by Macleods Pharma Usa Inc
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles, Rx Only, Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-165-90 UPC 3 72789 16590 5
by PD-Rx Pharmaceuticals, Inc.
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-164-90 UPC 3 72789 16490 8
by PD-Rx Pharmaceuticals, Inc.
- Reason
- CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- Published
- July 6, 2022
- 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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