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Recalls affecting Missouri

Data last updated: September 6, 2026 at 11:49 PM UTC

16,793 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
Wording
Class IHigh risk
FoodRecalled January 9, 2026

Modern Warrior Ready, Dietary Supplement, 60 CAPSULES

FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1178-2026
Lot/product code:
Product distributed between April of 2022 until December 8th of 2025.
Recalling firm:
Modern Warrior Life, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1106-2026
Lot/product code:
Product Number SMBARBO20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025289 and Use By 04/30/2027 Batch/Lot 025325 and Use By 05/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1102-2026
Lot/product code:
Product Number SMBARPD20001 Batch/Lot 025233 and Use By 08/31/2026 Batch/Lot 025237 and Use By 08/31/2026 Batch/Lot 025238 and Use By 08/31/2026 Batch/Lot 025239 and Use By 08/31/2026 Batch/Lot 025240 and Use By 08/31/2026 Batch/Lot 025241 and Use By 08/31/2026 Batch/Lot 025261 and Use By 09/30/2026 Batch/Lot 025265 and Use By 09/30/2026 Batch/Lot 025267 and Use By 09/30/2026 Batch/Lot 025268 and Use By 09/30/2026 Batch/Lot 025290 and Use By 10/31/2026 Batch/Lot 025294 and Use By 10/31/2026 Batch/Lot 025329 and Use By 11/30/2026 Batch/Lot 025330 and Use By 11/30/2026 Batch/Lot 025339 and Use By 12/31/2026 Batch/Lot 025343 and Use By 12/31/2026
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 23, 2025

Spice Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags

Not listed on the label Milk Allergen

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0499-2026
Lot/product code:
Batch 221
Recalling firm:
B.C. Williams Bakery Service, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 23, 2025

Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags

Not listed on the label Milk Allergen

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0500-2026
Lot/product code:
Lot #072225-217 Lot #072225-218 Lot #080325-200 Lot #080325-201 Lot #081625-203 Lot #081625-204 Lot #092225-222 Lot #092225-223 Lot #092225-224 Lot #092225-225 Lot #092225-226 Lot #092225-227 Lot #092225-228 Lot #101725-208 Lot #101725-209
Recalling firm:
B.C. Williams Bakery Service, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 23, 2025

Swiss Chocolate Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags

Not listed on the label Milk Allergen

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0501-2026
Lot/product code:
072925-220 and 071825-36
Recalling firm:
B.C. Williams Bakery Service, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 15, 2025

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of not listed on the label sildenafil and tadalafil

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0397-2026
Lot/product code:
All codes; Exp 12/31/2029
Recalling firm:
StuffbyNainax
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 12, 2025

ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0289-2026
Lot/product code:
All lots within expiry.
Recalling firm:
Medinatura New Mexico, inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 12, 2025

ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0288-2026
Lot/product code:
All lots within expiry.
Recalling firm:
Medinatura New Mexico, inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 8, 2025

Sam Dry Fruits & Nuts PISTACHIO Meats Whole LOT #: PK00459 NET WEIGHT: 30 LBS PACK DATE: AUGUST/2025 EXPIRATION DATE: AUGUST/2027

Potential contamination with Salmonella.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0357-2026
Lot/product code:
LOT #: PK00459
Recalling firm:
Sam Dry Fruits and Nuts Enterprises, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled November 8, 2025

1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets

Contaminated with Clostridium botulinum

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0249-2026
Lot/product code:
All batches and codes within expiry Finished Product Quantity 08NOV2023 to 08NOV2025 UPC Codes: Single Can: 8 50044 96800 8; Sams Club 2PK: 00850044968893; Amazon 2PK: 00850044968053; Anywhere pack: 8 50044 96802 2; 1-Count Sample Unit Anywhere Pack: 850044968015
Recalling firm:
ByHeart, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 6, 2025

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0182-2026
Lot/product code:
Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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.
View official FDA record (opens in a new tab)
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.
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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.
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)
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
View official FDA record (opens in a new tab)