UnclassifiedAnnounced September 4, 2026
Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement
Products contain undeclared yohimbine
Read FDA’s announcement (opens in a new tab)FDA food · drug · device recalls, merged
Before you eat it, take it, or plug it in — check.
Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.
Just announced
Straight from FDA press releases — not yet formally classified or risk-gradedUnclassifiedBacteria/virusAnnounced September 4, 2026
Foods Alive — Moringa Leaf Powder
Potential to be contaminated with Salmonella
Read FDA’s announcement (opens in a new tab)UnclassifiedAnnounced September 3, 2026
B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container
Presence of particulate matter identified as iron oxide
Read FDA’s announcement (opens in a new tab)UnclassifiedBacteria/virusAnnounced September 3, 2026
Great Value — Organic Triple Berry Blend
Possible E. Coli Contamination
Read FDA’s announcement (opens in a new tab)UnclassifiedAnnounced September 3, 2026
American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial
Presence of particulate matter and lack of sterility assurance
Read FDA’s announcement (opens in a new tab)UnclassifiedAnnounced August 31, 2026
Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement
Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)
Read FDA’s announcement (opens in a new tab)UnclassifiedAnnounced August 31, 2026
Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml
Contains garlic essential oil not approved for culinary use
Read FDA’s announcement (opens in a new tab)UnclassifiedAllergenAnnounced August 31, 2026
Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.
Undeclared milk
Read FDA’s announcement (opens in a new tab)UnclassifiedBacteria/virusAnnounced August 29, 2026
Everything Sprouts — Robust Radish Mix, 5oz Cups
Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.
Read FDA’s announcement (opens in a new tab)UnclassifiedBacteria/virusAnnounced August 29, 2026
Martina — Mangoes
Potential contamination with Salmonella
Read FDA’s announcement (opens in a new tab)Recalls nationwide
Data last updated: September 6, 2026 at 11:49 PM UTC
19,229 recalls foundClass IIILow risk
DrugRecalled August 16, 2023
Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg, 30 tablets, Rx only, Manufactured for: Esperion Therapeutics, Inc, Ann Arbor, MI 48108, NDC 72426-818-03
Failed dissolution specifications: below specification results at stability 12-month
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-1143-2023
- Lot/product code:
- Lot# 1904872, Exp 1/31/2025; 1950377, Exp 6/30/2025
- Recalling firm:
- Esperion
Class IIILow risk
DrugRecalled August 17, 2023
Sabril (vigabatrin) for Oral Solution, 500 mg, 50 Packets, Rx only, Manufactured by: Patheon, Cincinnati, OH 45237, NDC 67386-211-65
Cross contamination with other products
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-1142-2023
- Lot/product code:
- Lot#: 3207333A, 3207334A, Exp 03/2027; 3214707A, 3214709A, 3214710A, Exp 02/2028 .
- Recalling firm:
- Lundbeck LLC
Class IIILow risk
DrugRecalled September 22, 2023
Methotrexate Tablets, USP, 2.5 mg, 10x10 Unit-Dose Tablets per carton, Rx only, Distributed by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724. NDC: 0054-8550-25
Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0066-2024
- Lot/product code:
- Lot, expiry: Lot AB7486B, exp Dec 2023; Lot AB8766B, exp April 2024; Lot AB9484B, exp Aug 2024
- Recalling firm:
- West-Ward Columbus Inc
Class IIILow risk
DrugRecalled October 17, 2023
Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie Inc. North Chicago, IL 60064, U.S.A. NDC 0074-7068-11
Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0088-2024
- Lot/product code:
- Lot # 1187435 exp date: 02/2024
- Recalling firm:
- AbbVie Inc.
Class IIILow risk
DrugRecalled October 20, 2023
Oxaydo (oxycodone HCl, USP) tablets, 7.5 mg, 100 Tablets per bottle, Rx only, Distributed by: Zyla Life Sciences US Inc., Wayne, PA 19087. NDC: 69344-213-11
Weaker than it should be Drug: Lower potency than labeled.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0094-2024
- Lot/product code:
- Lot 22W02, Exp 01/31/2025
- Recalling firm:
- Zyla Life Sciences US Inc.
Class IIILow risk
DrugRecalled November 10, 2023
Tropicamide 1% (10mg/mL), Cyclopentolate 1% (10mg/mL), Phenylephrine 2.5% (25mg/mL), Ketorolac 0.5% (5mg/mL), 5 mL bottles, For Topical Ophthalmic Use Only, Not for IV Use, This is a Compounded Drug, Hospital & Office Use Only, Fagron Sterile Services, 8710 E 34th St N Wichita, KS 67226. NDC 71266-8240-01
Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the container is a 0.5mL single-use syringe instead of a 5 mL dropper
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0125-2024
- Lot/product code:
- Lot #: C274-000033372, Exp. Date 01-17-2024; C274-000033764, Exp. Date 02-06-2024
- Recalling firm:
- Fagron Compounding Services
Class IIILow risk
DrugRecalled November 20, 2023
Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain, Distributed by: Novartis Pharmaceuticals Corp., East Hanover, N.J. 07936, NDC 0078-1077-66
Failed Dissolution Specifications
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0149-2024
- Lot/product code:
- Lot# ME2713; Exp. 02/2025 Lot # MF8286, ML1860; Exp. 04/2025
- Recalling firm:
- Siegfried Barbera, SL
Class IIILow risk
DrugRecalled December 26, 2023
Benzonatate Capsules, USP, 100 mg, 100 Capsules (10 capsules x 10 unit dose cards), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC 68084-214-01; Individual Dose NDC 68084-214-11
Stronger than it should be drug: Assay results were slightly above specification at the time zero point.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0257-2024
- Lot/product code:
- Lot # 1014208, Exp Mar/31/2025
- Recalling firm:
- Amerisource Health Services LLC
Class IIILow risk
DrugRecalled January 18, 2024
Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01
Misprint on tablet
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0312-2024
- Lot/product code:
- Lot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026
- Recalling firm:
- Dr. Reddy's Laboratories, Inc.
Class IIILow risk
DrugRecalled January 18, 2024
Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-05
Misprint on tablet
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0313-2024
- Lot/product code:
- Lot: T2303609; Exp. 06/2026 Lot: T2303610; Exp. 06/2026
- Recalling firm:
- Dr. Reddy's Laboratories, Inc.
Class IIILow risk
DrugRecalled January 25, 2024
Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic regimen), packaged in cartons, each carton contains 6 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9012-58
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0322-2024
- Lot/product code:
- Lot #: 100040731, Exp 7/31/2024
- Recalling firm:
- Teva Pharmaceuticals USA, Inc
Class IIILow risk
DrugRecalled January 25, 2024
Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9008-67
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0321-2024
- Lot/product code:
- Lot #: 100042978, Exp 7/31/2024
- Recalling firm:
- Teva Pharmaceuticals USA, Inc
Class IIILow risk
DrugRecalled February 1, 2024
HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100-count (10 x 10) per unit dose carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-447-01; NDC Unit Dose: 68084-447-11
Failed Impurities/Degradation Specifications: not meeting quality requirements (OOS) result in the repackaged product for Related Compounds (Impurities) at the 6-month time point.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0320-2024
- Lot/product code:
- Lot #: 1012275, Exp 02/28/2025
- Recalling firm:
- Amerisource Health Services LLC
Class IIILow risk
DrugRecalled February 20, 2024
Clindamycin Phosphate Topical Solution USP, 1%, 60 mL bottle, Manufactured for: Glasshouse Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, L5N 6R8, NDC 71428-0003-60
Defective Container: not meeting quality requirements for weight due to a slow leakage at the 12-month stability timepoint.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0365-2024
- Lot/product code:
- Lot #: 119874; Exp 06/30/2025
- Recalling firm:
- Contract Pharmaceuticals Limited Canada
Class IIILow risk
DrugRecalled February 20, 2024
Clindamycin Phosphate, Topical Solution USP, 1%, 60 mL, Rx Only, Manufactured for and Distributed by: Marlex Pharmaceuticals, Inc., New Castle, DE 19720, NDC 10135-0691-61
Defective Container: not meeting quality requirements for weight due to a slow leakage at the 12-month stability timepoint.
ALL 50 STATES
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- D-0364-2024
- Lot/product code:
- Lot #: 119466, 119467 Exp 04/2025; 120351 Exp 08/2025; 121712 Exp 11/2025
- Recalling firm:
- Contract Pharmaceuticals Limited Canada
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES HASHBROWN CASSEROLE, ALLERGENS: MILK, WHEAT, SOY, FISH, PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label does not list the ingredients for their products.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1138-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES PEACH PIE INGREDIENTS: PEACH PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label fails list any sub ingredients.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1141-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the product label fails to list any sub ingredients.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1145-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES GREEN BEAN CASSEROLE, CONTAINS: MILK, SOY, FISH, WHEAT, PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label does not list the ingredients for their products.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1137-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES SQUASH CASSEROLE CONTAINS: MILK, EGGS, SOY, FISH, WHEAT PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the product label fails to list any ingredients.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1144-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES CHERRY PIE INGREDIENTS: CHERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR SPICES. CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label does not list the sub ingredients for their products.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1134-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES SWEET POTATO CASSEROLE CONTAINS: EGG, MILK PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the product label fails to list any ingredients.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1146-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES DOT'S POTATO BAKE 2lb INGREDIENTS: IDAHO POTATOES, MONT JACK, CHEDDAR, SHARP CHEEDAR, & CREAM CHEESES. SOUR CREAM, CHICKEN BROTH, BUTTER, CHIVES, SPICES. CONTAINS: MILK, SOY, FISH PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label fails to list any sub ingredients.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1142-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES Broccoli Casserole Contains: Wheat, Eggs, Milk, Soy, Fish PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label does not list any ingredients in the product.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1133-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises
Class IIILow risk
FoodRecalled March 26, 2024
PIES & SIDES CONNIE'S CARAMEL APPLE PIE 11 oz INGREDIENTS: APPLE PIE FILLING, SUGARS, VANILLA, CARAMEL EXTRACT BLEACHED FLOUR, SPICES, CONTAINS: WHEAT, PIES & SIDES MOUNT HOLLY, NC
During an inspection by NCDA, the firm was notified that the label does not list the sub ingredients for their products.
▸Full report
A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.
- Recall #:
- F-1135-2024
- Lot/product code:
- All lots shipped before 2/23/2024
- Recalling firm:
- Robeson Enterprises