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)Recalls affecting New Hampshire
Data last updated: September 6, 2026 at 11:49 PM UTC
16,278 recalls foundJust 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)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
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)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)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)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)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)UnclassifiedBacteria/virusAnnounced August 29, 2026
Martina — Mangoes
Potential contamination with Salmonella
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)Class IHigh risk
DrugRecalled October 29, 2025
POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0181-2026
- Lot/product code:
- Lot # 1030613, Exp Date: 09/30/2026
- Recalling firm:
- Otsuka ICU Medical LLC
Class IHigh risk
DrugRecalled October 29, 2025
POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0180-2026
- Lot/product code:
- Lot # 1030613, Exp Date: 09/30/2026
- Recalling firm:
- Otsuka ICU Medical LLC
Class IHigh risk
FoodRecalled October 24, 2025
Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775
Potential contamination of Salmonella Richmond
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0205-2026
- Lot/product code:
- 500-00055034; 500-00055035; 500-00055036; 500-00055037; 500-00055038; 500-00055039 500-00055040; 500-00055042; 500-00055043; 500-00055044; 500-00055045; 500-00055046 500-00055047; 500-00055048; 500-00055049; 500-00055050; 500-00055051; 500-00055052 500-00055053; 500-00055054; 500-00055055; 500-00055056; 500-00055057; 500-00055058 500-00056121; 500-00056122; 500-00056123; 500-00056124; 500-00056125; 500-00056126 500-00056127; 500-00056128; 500-00056129; 500-00056130; 500-00056131; 500-00056132 500-00056133; 500-00056134; 500-00056135; 500-00056136; 500-00056137; 500-00056138 500-00056139; 500-00056140; 500-00056141; 500-00056142; 500-00056143; 500-00056144 500-00056145; 500-00056146; 500-00056147; 500-00056148; 500-00056149; 500-00056150 500-00056151; 500-00056152; 500-00056153; 500-00056154; 500-00056155; 500-00056230 500-00056231; 500-00056318; 500-00056323; 500-00056429; 500-00056772;
- Recalling firm:
- MeriCal, LLC
Class IHigh risk
DrugRecalled October 20, 2025
SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of not listed on the label meloxicam.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0388-2026
- Lot/product code:
- All lots within expiry
- Recalling firm:
- ANTHONY TRINH, 123Herbals LLC
Class IHigh risk
DrugRecalled October 8, 2025
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
Marketed Without an Approved NDA/ANDA-FDA analysis revealed not listed on the label sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0396-2026
- Lot/product code:
- ALL LOTS, exp 12/31/2027
- Recalling firm:
- Mohamed Hagar
Class IHigh risk
DrugRecalled September 16, 2025
Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1
Weaker than it should be Drug: Testing revealed there was no oxytocin in the IV bag.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0015-2026
- Lot/product code:
- Lot #: 20250620OXY-1, Expiration date 10/18/2025
- Recalling firm:
- IntegraDose Compounding Services LLC
Class IHigh risk
FoodRecalled September 10, 2025
GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAITAKE MUSHROOM, SHIITAKE MUSHROOM]), VEGAN WHITE CHEDDAR CHEESE (DRIED CASHEW MILK [CASHEWS, CHICORY ROOT FIBER], NATURAL FLAVOR, NUTRITIONAL YEAST, TAPIOCA FLOUR, PEA PROTEIN, LACTIC ACID, DRIED APPLE CIDER VINEGAR, GARLIC). CONTAINS WHEAT AND CASHEWS Distributed by Gooder Foods Inc. Santa Cruz, CA 95060
Not listed on the label allergens (milk).
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0027-2026
- Lot/product code:
- Lots: 09725N, 09825N, 09925N, 10025N, 10125N UPC: 850031990074 BEST IF USED BY: Jul-07-2026, Jul-08-2026, Jul-09-2026, Jul-10-2026, Jul-11-2026
- Recalling firm:
- Gooder Foods, Inc.
Class IHigh risk
FoodRecalled September 10, 2025
GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS NET WT 6 OZ (170g) INGREDIENTS: GOODLES SHELLS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAITAKE MUSHROOM, SHIITAKE MUSHROOM]), CHEDDAR AND PARMESAN CHEESES (CULTURED MILK, SALT, DISODIUM PHOSPHATE, ENZYMES), WHEY, NATURAL FLAVOR, BUTTER (CREAM, SALT), NONFAT DRY MILK, SALT, TAPIOCA FLOUR, NUTRITIONAL YEAST, LACTIC ACID, PORCINI MUSHROOMS, BLACK PEPPER, PAPRIKA, GROUND BALCK TRUFFLES. CONTAINS WHEAT AND MILK Distributed by Gooder Foods Inc. Santa Cruz, CA 95060
Not listed on the label allergens (cashews).
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0028-2026
- Lot/product code:
- Lots: 10125 N, 10425 N, 10525 N UPC: 850031990159 BEST IF USED BY: Jul-11-2026, Jul-14-2026, Jul-15-2026
- Recalling firm:
- Gooder Foods, Inc.
Class IHigh risk
DrugRecalled August 28, 2025
Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0304-2026
- Lot/product code:
- LOT308EXP03/28
- Recalling firm:
- Green Lumber Holdings, LLC
Class IHigh risk
DrugRecalled August 27, 2025
Cyclobenzaprine Hydrochloride Tablets, USP, 10 mg, 90-count bottle, RX only, Manufactured by: Unichem Laboratories, Ltd, Pilerne Ind. Estate, Pilerne, Bardez, Goa, India; Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ. NDC 29300-415-19.
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0655-2025
- Lot/product code:
- Lot No: GMML24026A, Expires: 09/30/2027
- Recalling firm:
- Unichem Pharmaceuticals USA Inc.
Class IHigh risk
DrugRecalled August 18, 2025
Lactated Ringers's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07
Presence of Particulate Matter
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0627-2025
- Lot/product code:
- Lot #: J4S807, Exp 5/31/2027
- Recalling firm:
- B BRAUN MEDICAL INC
Class IHigh risk
DrugRecalled August 18, 2025
0.9% Sodium Chloride Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7800-09
Presence of Particulate Matter.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0628-2025
- Lot/product code:
- Lot #: V3K770, Exp 1/31/2026
- Recalling firm:
- B BRAUN MEDICAL INC
Class IHigh risk
DrugRecalled July 30, 2025
NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Microbial Contamination of Sterile Products: elevated endotoxin levels
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0094-2026
- Lot/product code:
- Lot#: GG121624-023, within expiry
- Recalling firm:
- GenoGenix LLC
Class IHigh risk
FoodRecalled July 25, 2025
Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES NET WT 5.6OZ (160g) NO ADDED SWEETENERS ONE INGREDIENT ONLY PER PACK UPC 1 93968 50900 2
Listeria monocytogenes. During routine testing the firm received positive test results for Listeria monocytogenes.
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0394-2025
- Lot/product code:
- Best By: 06/24/2027 25175; Best By: 06/25/2027 25176; Best By: 06/26/2027 25177; Best By: 06/30/2027 25181; Best By: 07/01/2027 25182; Best By: 07/02/2027 25183; Best By: 07/03/2027 25184; Best By: 07/05/2027 25186; Best By: 07/07/2027 25188; Best By: 07/08/2027 25189; Best By: 07/09/2027 25190; Best By: 07/10/2027 25191; Best By: 07/11/2027 25192; Best By: 07/15/2027 25196; Best By: 07/16/2027 25197; Best By: 07/27/2027 25198; Best By: 07/18/2027 25199; Best By: 07/21/2027 25202; Best By: 07/22/2027 25203; Best By: 07/23/2027 25204; Best By: 07/24/2027 25205; Best By: 07/25/2027 25206
- Recalling firm:
- Doehler North America, Inc.
Class IHigh risk
DrugRecalled July 17, 2025
DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.) bag-n-box (NDC 61924-092-27) and b) 1000ml (34 fl. oz.) bag-n-box (NDC 61924-092-34) , DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0610-2025
- Lot/product code:
- Lot # and Expiration Date: a) 30550A, Exp. Date 7/2025; 30670A, 30682A, Exp. Date 8/2025; 40025A, Exp. Date 1/2026; 40375A, Exp. Date 4/2026; 40427A, 40436A, Exp. Date 5/2026; 50068A, Exp. Date 1/2027. b)30586A, 30586B, 30626A, Exp. Date 7/2025; 30628A, 30657A, Exp. Date 8/2025; 30741A, Exp. Date 7/2025; 30871A, Exp. Date 10/2025; 40002A, Exp. Date 12/2025; 40012A, Exp. Date 1/2026; 40301A, Exp. Date 3/2026; 40789 A, Exp. Date 9/2026; 50068B, Exp. Date 1/2027; 50144A, 50149A, Exp. Date 2/2027.
- Recalling firm:
- DermaRite Industries, LLC
Class IHigh risk
DrugRecalled July 17, 2025
KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0612-2025
- Lot/product code:
- Lot #: 30705A, Exp. Date 8/2025; 30771A, Exp. Date 9/2025; 30920A, Exp. Date 10/2025; 40016A, Exp. Date 1/2026; 40303A, Exp. Date 4/2026; 40428A, Exp. Date 5/2026; 40505A, Exp. Date 6/2026; 41053C, 41053A, 41053B, Exp. Date 12/2026, 50017A, Exp. Date 1/2027.
- Recalling firm:
- DermaRite Industries, LLC
Class IHigh risk
DrugRecalled July 17, 2025
PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0613-2025
- Lot/product code:
- Lot #: 31013A, Exp. Date 11/2025; 40345A, 40355A, Exp. Date 4/2026; 40571A, 40580A, Exp. Date 6/2026; 40587A, 40591A, Exp. Date 7/2026; 40870.1, 40877.1, Exp. Date 10/2026; 41093A, Exp. Date 12/2026; 50072A, 50079A, Exp. Date 1/2027
- Recalling firm:
- DermaRite Industries, LLC
Class IHigh risk
DrugRecalled July 17, 2025
DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0611-2025
- Lot/product code:
- Lot #: 40187.2, Exp. Date 2/2026
- Recalling firm:
- DermaRite Industries, LLC
Class IHigh risk
FoodRecalled July 14, 2025
Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik Urunlerilkl. Gida Turkey
Salmonella. The firm was notified by the FDA that the product may be contaminated with Salmonella.
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0305-2025
- Lot/product code:
- BEST BEFORE: APRIL 01 2027; BATCH NUMBER: 250401
- Recalling firm:
- World Market Management Services, LLC
Class IHigh risk
DrugRecalled June 27, 2025
Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781-6136-94.
Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0570-2025
- Lot/product code:
- Lot # PG4360, PG4362, Exp. 11/30/2027
- Recalling firm:
- Sandoz Inc
Class IHigh risk
DrugRecalled June 27, 2025
Cefazolin for Injection, USP, 1 gram per vial, Sterile, For Intramuscular or Intravenous Use, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781 3451-70 (vial), NDC: 0781-3451-96 (carton).
Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained Cefozalin
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0569-2025
- Lot/product code:
- Lot # PG4360, PG4362, Exp. 11/30/2027
- Recalling firm:
- Sandoz Inc
Class IHigh risk
FoodRecalled June 16, 2025
D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.
Not listed on the label milk allergen
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0136-2026
- Lot/product code:
- D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds) o Lot #(s) 204214-RL, 204214, 204215, 224221, 224222, 224223, 135215, 135216, 135217, 135220, 135221, 145204, 145205-1, 145207-1, 145210-1
- Recalling firm:
- Weaver Nut Company, Inc
Class IHigh risk
FoodRecalled June 16, 2025
47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.
Not listed on the label milk allergen
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- H-0135-2026
- Lot/product code:
- 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) o Lot #(s): 204206, 204207, 204208, 204209, 204212, 224225
- Recalling firm:
- Weaver Nut Company, Inc
Class IHigh risk
DrugRecalled June 6, 2025
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0505-2025
- Lot/product code:
- All Lots.
- Recalling firm:
- Church & Dwight Inc
Class IHigh risk
DrugRecalled June 6, 2025
Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.
Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.
ALL 50 STATES
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0506-2025
- Lot/product code:
- All Lots.
- Recalling firm:
- Church & Dwight Inc