FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- H&R Flour, UNBL, EN, MT / Product Code 706220 in 50# bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- H & R All Purpose Flour BL EN MT /Product Code: 706250 in 50…
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- H & R All Purpose Flour MT/Product Code: 706205 in 50 lbs ba…
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Commander Flr BL ENR BR MT, Product Code 704260 in 50 lbs…
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Commander Flour, Product Code 704220 in 50 lbs bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Bova Flour HG, Product Code 804207 in 50 lbs bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Best Baker's flour 50 lbs bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Balancer flour 50 lbs bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- PB 25 LBS All Purpose Flour Product Code 806326
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- King Arthur All Purpose Flour 25# bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Robin Hood All-purpose Flour in 5 lb bag UPC 051500180105
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- King Arthur All-purpose Flour in 5 lb bag UPC 071012010509
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Adm Milling
- Product
- Bakers Corner All Purpose Flour in 5 lb. bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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FDA Recall
🇺🇸 United States
Completed
Historical recordClass II
Market America Inc
- Product
- bliss anti-stress formula Dietary Supplement, 60 Tablets; Ma…
- Reason
- Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.
- Published
- February 19, 2020
- Distribution
- Product was shipped to the following sta…
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FDA Recall
Terminated
Historical recordClass III
Pioglitazone and Metformin Hydrochloride Tablets, USP 15 mg/500 mg, Rx Only, 60-count bottle, Manufactured for Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, India, NDA 33342-176-09
by Macleods Pharma Usa Inc
- Reason
- Subpotent Drug: Out of specification assay result, below specification, for two lots of Pioglitazone And Metformin Hydrochloride Tablets.
- Published
- February 12, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009 USA; Manufactured By: Graviti Pharmaceuticals Pvt. Ltd., Telangana -502307, INDIA; NDC 70377-027-11.
by Graviti Pharmaceuticals Private Limited
- Reason
- Presence of Foreign Tablets/Capsules: Customer complaint that one 20 mg Atorvastatin Calcium Tablet was present in a bottle labeled as and containing eight-nine Atorvastatin Calcium Tablets, USP 10 mg.
- Published
- February 12, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2465-01
by Teva Pharmaceuticals USA
- Reason
- GMP Deviations: Product bottle may be absent of desiccant.
- Published
- February 12, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01
by Teva Pharmaceuticals USA
- Reason
- GMP Deviations: Product bottle may be absent of desiccant.
- Published
- February 12, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Clonidine Hydrochloride Tablets, USP 0.1mg, Rx Only, 100-count bottle, Manufactured by: Unichem Laboratories Ltd. Pilerne Ind. Estate, Pilerne Bardez, Goa 403 511 India. Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ 08816. NDC 29300-135-01
by UNICHEM PHARMACEUTICALS USA INC
- Reason
- Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container label.
- Published
- February 12, 2020
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass II
Olmesartan Medoxomil Tablets 20 mg, Rx Only, 90 Tablets per Bottle, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013 INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054, NDC 67877-446-90.
by Ascend Laboratories LLC
- Reason
- cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error with alternate API source prior to filing and approval of Prior Approval Supplement.
- Published
- February 12, 2020
- 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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