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Recalls affecting Tennessee

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

17,051 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

Jalapeno Cheese packaged as: (a) Deli Readi Jalapeno St Pk 1oz Slice, Item 10831, 2 lbs, UPC 634660628788

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-1709-2017
Lot/product code:
Lot Numbers: (a) 2/28/2017, 4/22/2017, 5/18/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Colby Cheese packaged as follows: (a) AMISH CLASSICS, DELI HORN, Item 55209, NET WT 6 LBS, UPC 0 08 28653 55209 3 (b) AMISH CLASSICS, FULLMOON(R), Item 55241, approximately 8 oz, UPC 828653552413 (c) AMISH CLASSICS EW FULL MOON, ITEM 55245, 8 oz, UPC 828653552451 (d) 8/2# RW Deli Readi Colby Mini Cheese Slices, ITEM 55831, 2 lbs., UPC 634660 628597 (e) Deli Made EZ(R) Slices, NET WT1.5 LB (681g), Item 55553, UPC 8 28653 55554 4 (f) Meijer Colby Cheese DELI HORN, Item 55755, 6 lbs., no UPC (g) Amish Classics Colby RW Halfmoon, Item 55244, 8 oz, no UPC (h) Meijer Colby EW Halfmoon, Item 55758, 8 oz, UPC 7 13733 34047 2 (i) RW Deli Readi Colby 1/2 Moon Slices, Item 55830, 1 lb, UPC 6 34660 62872 6 (j) Old Tyme Colby EW Halfmoon, Item 55703, 8 oz, UPC 8 28653 10555 8 (k) AMISH CLASSICS Colby Longhorn, Item 55523, 15 lbs, no UPC (l) Dietz & Watson Colby Mini Horn, Item 55740, 6 lbs, no UPC (m) Troyer Colby EW Halfmoon, Item 55840, 8 oz, UPC 04964693609 (n) Troyer Colby EW Full Moon, Item 55841, 8 oz, UPC 049646936045 (o) Troyer Colby RW Halfmoon, Item 55842, 8 oz, no UPC

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-1694-2017
Lot/product code:
(a) Lot Numbers: Sell By: 02/28/2017 through 08/14/2017 (b) Lot Numbers: Best if Used By: 02/28/2017 through 08/14/2017 (c) Lot Numbers: Best if Used By: 02/28/2017 through 08/14/2017 (d) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (e) Lot number 335-16, Best if used by: 02/28/2017 through 08/14/2017 (f) Lot Numbers: Sell by Date: 05/02/2017, 02/28/2017 through 08/14/2017 (g) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (h) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (i) Lot Numbers: USE BY: 02/28/2017 through 08/14/2017 (j) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (k) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (l) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (m) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (n) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (o) Lot Numbers: 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

Hot Pepper Cheese packaged as: (a) AMISH CLASSICS Hot Pepper RW Square, Item 26244, 12 lbs, UPC 858653262442 (b) Deli Made EZ Hot Pepper St Pk .5oz, Item 26555, 1.5 lbs, UPC 828653265559 (c) Deli Readi Hot Pepper St Pk 1oz Slice, Item 26831, 2 lbs, UPC 634660628788 (d) LIPARI Old Tyme Hot Pepper Cheese Food EW Square, Item 26703, 8 oz, UPC 94776102280

Potential cross contamination from a sample 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-1697-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 6/10/2017 (b) Best if Used by: 3/17/2017, 4/22/2017 (c) Best if Used by: 2/28/2017, 4/22/2017, 5/16/2017 (d) Best if Used by: 6/10/2017
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 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
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 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 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
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
▸Full report

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-P 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-1277-2026
Lot/product code:
Lot Code Format = MMD,DYY: 120,623. 031,824. 070,324. 100,224. 041,425. 101,625.
Recalling firm:
Byron White Formulas, Inc.
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)
Class IIModerate risk
FoodRecalled August 11, 2026

Byron White FORMULAS A-L Complex 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-1276-2026
Lot/product code:
Lot Code Format = MMD,DYY: 012,324. 041,924. 062,824. 092,024. 101,624. 111,324. 071,425. 093,025. 012,026. 042,826.
Recalling firm:
Byron White Formulas, Inc.
View official FDA record (opens in a new tab)