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Recalls affecting Missouri

Data last updated: September 8, 2026 at 1:13 PM UTC

16,966 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

▸Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View 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

▸Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View 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

▸Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

▸Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View 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

▸Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

▸Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View 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.

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
NewestOldest
High riskLow riskAll
Wording
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Havarti Cheese Packaged as: (a) AMISH CLASSICS Deli Made EZ Havarti .75oz St Pk Slice, Item 71554, 1.5 lbs, UPC 82853715542

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1708-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 5/3/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Mozzarella Cheese packaged as: (a) Deli Made EZ Mozzarella St Pk .75oz Slice, Item 11553, 1.5 lbs, UPC 828653105558

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1705-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 322-16, 333-16
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Pepper Jack Cheese packaged as: (a) Troyer Pepper Jack EW Halfmoon, Item 10840, 8 oz, UPC 49646936106 (b) Troyer Pepper Jack EW Full Moon, Item 10841, 8 oz, UPC 49646936069

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1710-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Jalapeno Jack cheese packaged as follows: (a) AMISH CLASSICS Jalapeno Jack Mini Horn, Item 10209, 6 lbs, No UPC (b) AMISH CLASSICS Jalapeno Jack RW Fullmoon, Item 10241, 12 lbs, no UPC (c) AMISH CLASSICS Jalapeno Jack RW Halfmoon, Item 10244, 12 lbs, no UPC (d) AMISH CLASSICS Jalapeno Jack EW Fullmoon, Item 10245, 8 oz, UPC 828653102458 (e) AMISH CLASSICS Jalapeno Jack Cheese, Item 10311, 10 lbs, no UPC 10 lbs, no UPC (f) Deli Made EZ Jalapeno Jack St Pk .75 oz Slice, Item 10553, 1.5 lbs, no UPC (g) Deli Made EZ Jalapeno Jack St Pk .75 oz Slice, Item 10554, 1.5 lbs, UPC 828653105541 (h) Deli Made EZ Jalapeno Jack St Pk .5 oz Slice, Item 10555, 1.5 lbs, UPC 828653105558 (i) LIPARI Old Tyme Jalapeno Jack EW Halfmoon, Item 10703, 8 oz, UPC 94776102303 (k) Sutters Quality Foods Jalapeno Jack St Pk .75oz Slice, Item 10812, 1.5 lbs, UPC 828653108122 (l) Sutters Quality Foods Jalapeno Jack Loaf, Item 10815, 5 lbs, no UPC (n) Winder Farms Jalapeno Jack St Pk .75oz Slice, Item 10790, 1 lb, UPC 828653107903

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1696-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017 (d) Best if used by: 02/28/2017 through 08/14/2017 (e) Best if Used by: 4/18/2017 (f) Best if Used by: 003-17 (g) Best if Used by: 3/17/2017, 5/3/2017 (h) Best if Used by: 3/28/2017, 3/30/2017, 5/18/2017 (i) Best if Used by: 5/29/2017 (j) Best if Used by: 2/28/2017, 5/16/2017 (k) Best if Used by: 5/9/2017 (l) Best if Used by: 5/3/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Cheddar Cheese packaged as: (a) AMISH CLASSICS Cheddar Mild Color, Item 28311, 10 lbs, No UPC (b) Deli Made EZ Cheddar Mild Stick, Item 28532, 4.5 lbs, no UPC (c) Deli Made EZ Cheddar Mild C St Pk .75oz Slice, Item 28545, 2 lbs, UPC 828653285458 (d) AMISH CLASSICS Deli Made EZ Cheddar St Pk .75oz Slice, Item 28553, 1.5 Lbs, no UPC (e) AMISH CLASSICS Deli Made EZ Cheddar Mild Stk Pk .5oz Slice, Item 28555, 1.54 lbs, UPC 828653285557 (f) Deli Readi Cheddar St Pk 1oz Slice, Item 28831, 2 lbs, UPC 634660628771 (g) Duck Deli Cheddar Mild Color Loaf, Item 28745, 5 lbs, no UPC (h) Duck Deli Cheddar st pk .75oz Slice, Item 28747, 1.5 lbs, UPC 828653287476 (i) Madison Valley Farms Cheddar St Pk .75oz Slice, Item 28769, 1.5 lbs, UPC 828653287698 (j) Sutters Quality Foods Cheddar St Pk .75oz Slice, Item 28812, 1.5 lbs, UPC 828653288126 (k) Sutters Quality Foods Cheddar Mild Color Loaf, Item 28815, 5 lbs, no UPC (l) Troyer Cheddar EW Full Moon, Item 28841, 8 oz, UPC 49646936076

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1702-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 3/28/2017, 4/25/2017, 5/26/2017, 7/3/2017 (b) Best if Used by: 4/18/2017 (c) Best if Used by: 4/22/2017 (d) Best if Used by: 018-17 (e) Best if Used by: 3/10/2017, 4/22/2017 (f) Best if Used by: 2/28/2017, 5/4/2017 (g) Best if Used by: 273-16 (h) Best if Used by: 004-17, 358-16 (i) Best if Used by: 320-16 (j) Best if Used by: 5/18/2017 (k) Best if Used by: 4/18/2017 (l) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Monterey Jack Cheese packaged as: (a) AMISH CLASSICS Deli Made EZ Monterey Jack St Pk .75 oz Slice, Item 03554, 1.5 lbs, UPC 828653035541

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1704-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 3/28/2017, 5/3/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 4, 2016

Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1159-02

Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.

ALL 50 STATES
▸Full report

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

Recall #:
D-0218-2017
Lot/product code:
Lot # 59064DK, Exp. 11/17
Recalling firm:
Hospira Inc., A Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 2, 2016

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.

ALL 50 STATES
▸Full report

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

Recall #:
D-0918-2017
Lot/product code:
Lot # 22016, Exp 1/30/2017
Recalling firm:
Complete Pharmacy and Medical Solutions LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 23, 2016

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

Presence of Particulate Matter: Confirmed customer complaint for the 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-1137-2016
Lot/product code:
Lot #: 50-343-DK*, Exp 01FEB2017; note that the lot number may be followed by numbers from 01 to 99.
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 18, 2016

8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02

Presence of Particulate Matter: particulate matter identified as an insect in one vial.

ALL 50 STATES
▸Full report

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

Recall #:
D-0865-2016
Lot/product code:
Lot # 56-148-EV, Exp 8/1/2017
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 23, 2015

APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.

Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0667-2016
Lot/product code:
All lots
Recalling firm:
Nuway Distributors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled August 27, 2015

MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7 538073516768.

Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain not listed on the label phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0230-2016
Lot/product code:
All lots through Expiration Date 04/15/2018
Recalling firm:
The One Minute Miracle Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled August 27, 2015

MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules per carton, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 0911312397354.

Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain not listed on the label thiosildenafil, an analogue of an FDA approved drug for male erectile dysfunchtion making this product an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0229-2016
Lot/product code:
All lots through Expiration Date 06/01/2018
Recalling firm:
The One Minute Miracle Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled July 13, 2015

Akttive High Performance Fat Burner Gold dietary supplement capsules, 30-count bottle, Distributed by Life and More, L.L.C., Doral, Florida

Marketed Without An Approved NDA/ANDA: Dietary supplements contains not listed on the label sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling.

ALL 50 STATES
▸Full report

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

Recall #:
D-0664-2016
Lot/product code:
Lot # 000815004400; Exp 12/17
Recalling firm:
Life and More LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 2, 2015

Zero Xtreme High Performance Fat Burner capsules, 30-count bottle, Distributed by Xtreme Z Distributors, Inc., Miami, FL 33180

Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed the presence of sibutramine and desmethylsibutramine.

ALL 50 STATES
▸Full report

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

Recall #:
D-1165-2016
Lot/product code:
Lot 1220062085, Exp. 09/16
Recalling firm:
XTREME Z DISTRIBUTORS INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled September 10, 2012

HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-3888-21

Stronger than it should be (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in stronger than it should be assays of both the hydrocodone and acetaminophen components.

ALL 50 STATES
▸Full report

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

Recall #:
D-057-2013
Lot/product code:
Lot number: C1440512A, Exp 12/13
Recalling firm:
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 24, 2026

Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33432, Manufactured by: West-Ward Columbus Inc., Columbus, OH 43228.

Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0831-2026
Lot/product code:
a) Lot #: AC5470A, Exp. Date July 2027 b) Lot #: AC5470B, Exp. Date July 2027
Recalling firm:
Hikma Pharmaceuticals USA INC.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled August 18, 2026

Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Foreign object: products may contain glass pieces

ALARAZCACOCTFLGAIAIDILKSLAMAMDMIMNMONCNDNHNJNVNYOHPAPRTNTXUTVAVIWAWI
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1266-2026
Lot/product code:
Batch code/ Best Before (bottom of package): LLA616803 30 SEP 2027 LLA616903 30 SEP 2027 LLA619703 31 OCT 2027 UPC Bottom of package: 041548244044 LLA619803 31 OCT 2027 LLA619903 31 OCT 2027 LLA620003 31 OCT 2027 LLA620103 31 OCT 2027 LLA620203 31 OCT 2027 LLA620303 31 OCT 2027
Recalling firm:
Dreyer's Grand Ice Cream Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled August 18, 2026

Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 041548612041, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Foreign object: products may contain glass pieces

ALARAZCACOCTFLGAIAIDILKSLAMAMDMIMNMONCNDNHNJNVNYOHPAPRTNTXUTVAVIWAWI
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1267-2026
Lot/product code:
Batch code/ Best Before (bottom of package): LLA619603 31 OCT 2027 LLA619703 31 OCT 2027
Recalling firm:
Dreyer's Grand Ice Cream Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled August 18, 2026

Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Foreign object: products may contain glass pieces

ALARAZCACOCTFLGAIAIDILKSLAMAMDMIMNMONCNDNHNJNVNYOHPAPRTNTXUTVAVIWAWI
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1265-2026
Lot/product code:
Batch code/ Best Before (bottom of package): LLA617603 30 JUN 2027 LLA617703 30 JUN 2027 LLA617803 30 JUN 2027 LLA617903 30 JUN 2027 LLA618003 30 JUN 2027 LLA618103 30 JUN 2027 LLA618203 31 JUL 2027 LLA618303 31 JUL 2027 LLA618403 31 JUL 2027 LLA618503 31 JUL 2027 LLA619003 31 JUL 2027 LLA619103 31 JUL 2027 LLA619203 31 JUL 2027 LLA619303 31 JUL 2027 LLA619403 31 JUL 2027 LLA619503 31 JUL 2027
Recalling firm:
Dreyer's Grand Ice Cream Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled August 18, 2026

Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Foreign object: products may contain glass pieces

ALARAZCACOCTFLGAIAIDILKSLAMAMDMIMNMONCNDNHNJNVNYOHPAPRTNTXUTVAVIWAWI
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1268-2026
Lot/product code:
Batch code/ Best Before (bottom of package): LLA618503 31 JUL 2027 LLA618603 31 JUL 2027 LLA618703 31 JUL 2027 LLA618803 31 JUL 2027 LLA618903 31 JUL 2027 LLA619003 31 JUL 2027
Recalling firm:
Dreyer's Grand Ice Cream Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled August 18, 2026

Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Foreign object: products may contain glass pieces

ALARAZCACOCTFLGAIAIDILKSLAMAMDMIMNMONCNDNHNJNVNYOHPAPRTNTXUTVAVIWAWI
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1264-2026
Lot/product code:
Batch code/ Best Before (bottom of package): LLA616903 30 SEP 2027 LLA617003 30 SEP 2027 LLA617103 30 SEP 2027 LLA617203 30 SEP 2027 LLA617303 30 SEP 2027 LLA617403 30 SEP 2027 LLA617503 30 SEP 2027 LLA617603 30 SEP 2027 LLA620303 31 OCT 2027 LLA620403 31 OCT 2027 LLA620503 31 OCT 2027 LLA620603 31 OCT 2027 LLA620703 31 OCT 2027 LLA620803 31 OCT 2027 LLA620903 31 OCT 2027 LLA621003 31 OCT 2027 LLA621103 31 OCT 2027 LLA621203 31 OCT 2027 LLA621303 30 NOV 2027 LLA621403 30 NOV 2027 LLA621503 30 NOV 2027 LLA621603 30 NOV 2027
Recalling firm:
Dreyer's Grand Ice Cream Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled August 18, 2026

Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Foreign object: products may contain glass pieces

ALARAZCACOCTFLGAIAIDILKSLAMAMDMIMNMONCNDNHNJNVNYOHPAPRTNTXUTVAVIWAWI
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1269-2026
Lot/product code:
Batch code/ Best Before (bottom of package: LLA603840 31 MAY 2027 LLA605540 31 MAY 2027 LLA605640 31 MAY 2027 LLA605740 31 MAY 2027 LLA605940 31 MAY 2027
Recalling firm:
Dreyer's Grand Ice Cream Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 13, 2026

Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-4379-3

Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria

ALL 50 STATES
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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0804-2026
Lot/product code:
Lot # TY9494, Exp Date: 05/31/2027.
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled August 11, 2026

Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404

Label does not declare walnuts in English

AKALARAZCACOCTDCDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMTNCNENHNJNMNVNYOHOKORPAPRRISCSDTNTXUTVAVTWAWIWVWY
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1278-2026
Lot/product code:
Lot Code Format = MMD,DYY: 022,224. 061,424. 092,324. 022,125. 071,825. 112,125. 040,826.
Recalling firm:
Byron White Formulas, Inc.
View official FDA record (opens in a new tab)