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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded

Recalls nationwide

Data last updated: September 6, 2026 at 10:21 PM UTC

19,229 recalls found
Wording
Class IHigh risk
FoodRecalled February 24, 2017

7-Eleven, Mantecada MUFFIN, Net Wt. 4 oz. , UPC 05254859241-7, in clear flexible plastic, Distributed by 7-Eleven, Inc., Irving, TX 750634.

Not listed on the label Allergen: Milk

Full report

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

Recall #:
F-1912-2017
Lot/product code:
UPC 05254859241-7, SKU #9841
Recalling firm:
Bak EZ
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 9, 2017

Soynut Butter repackaged into smaller containers and labeled. Container amounts vary according to how servings are needed per order. Each serving size is 0.56 oz.. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1953-2017
Lot/product code:
Product Code 8458. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 9, 2017

Whole Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1951-2017
Lot/product code:
Product Code 8465. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 9, 2017

Half Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1950-2017
Lot/product code:
Product Code 8464. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 9, 2017

Portion cup of soynut butter served with other food items such as milk, yogurt, raisins, and gold fish crackers, labeled and served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1952-2017
Lot/product code:
Product Code 8743. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 9, 2017

Pan Pita with soynut butter spread on top, 4" pita. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1949-2017
Lot/product code:
Product Code 8491. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 12, 2017

EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

ALL 50 STATES
Full report

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

Recall #:
D-0691-2017
Lot/product code:
US lot 5GN767, expiration April 2017; lot 5GN773, expiration April 2017; lot 6GN215, expiration Sep 2017: INTERNATIONAL lot 5GR765, expiration March 2017; lot 5GK771, expiration April 2017; lot 5ED824, expiration April 2017; and lot 6ED117, expiration ***
Recalling firm:
Meridian Medical Technologies a Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 12, 2017

EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

ALL 50 STATES
Full report

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

Recall #:
D-0690-2017
Lot/product code:
US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017; lot 6GM088, exp. Oct 2017; lot 6GM087, exp. Oct 2017; lot 6GM198, exp. Oct 2017; lot 6GM081, exp. Sep 2017; lot 6GM091, exp. Oct 2017; lot 6GM199, exp. Oct 2017: INTERNATIONAL: lot 5FA665, exp. April 2017; lot 5GU763, exp. May 2017; lot 6FA293, exp. Oct 2017; lot 6FA292, exp. Oct 2017; lot 6GH294, exp. Oct 2017.
Recalling firm:
Meridian Medical Technologies a Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Ham & Cheddar sandwiches. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2087-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Ham and Turkey 12" sub. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2091-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Turkey wedge sandwich. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2085-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Italian sub, 12". Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2090-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Black Forest Ham and Cheddar sandwiches. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2088-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Turkey and Havarti sandwiches. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2086-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Roast Beef Sandwich. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2092-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Italian Sub, Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2089-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 20, 2017

Cuban Sandwich. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2093-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 21, 2017

Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10

Presence of Particulate Matter: human hair found within an internal sample syringe.

ALL 50 STATES
Full report

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

Recall #:
D-0862-2017
Lot/product code:
Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled May 11, 2017

Queso Fresco x LB (Barra)/ Whole Milk Cheese, Net Wt 5-6 lbs.

Product contaminated with Listeria monocytogenes

Full report

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

Recall #:
F-2410-2017
Lot/product code:
Exp 06/17/2017, no UPC
Recalling firm:
Global Garlic, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled May 11, 2017

De Mi Pais, Queso Fresco, Whole Milk Cheese, Net Wt 16 oz.. (1 lb)

Product contaminated with Listeria monocytogenes

Full report

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

Recall #:
F-2409-2017
Lot/product code:
Exp 09/19/2017, UPC 8-96211-00235-9
Recalling firm:
Global Garlic, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 6, 2018

Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce; Net Wt. 18 oz. bottle; UPC Code 0 7561654383 8

Not listed on the label soy and wheat ingredients

ALL 50 STATES
Full report

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

Recall #:
F-0978-2018
Lot/product code:
All lots
Recalling firm:
Piggie Park Enterprises Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 13, 2018

Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

Shell eggs have the potential to be contaminated with Salmonella Braenderup.

Full report

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

Recall #:
F-1410-2018
Lot/product code:
Plant Number P-1065; LOT CODES with a Julian date ranged from 011 - 102; Numerous UPCs
Recalling firm:
ROSE ACRE FARM
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 19, 2018

Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc. Batavia, IL 60510; Product of USA; Manufactured In A Facility That Processes Peanuts and Soy. May Contain Peanuts and Soy. Packaged in a steel 2-piece can.

Canned spinach is being recalled due to the potential to contain boiled peanuts instead of spinach.

Full report

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

Recall #:
F-1412-2018
Lot/product code:
Lot Code: SPIN71A23IX Use by January 2021; UPC: 041498131289
Recalling firm:
Mccall Farms Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 27, 2018

Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOY FLOUR),***RICE FLOUR,***SUNFLOWER AND/OR SOY LECITHIN***CONTAINS: SOY DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS SAN DIEGO, CA 92154 UPC 0 89947 30206 4

The firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.

Full report

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

Recall #:
F-1475-2018
Lot/product code:
Lot Code #A640234710 WL2, BEST BY AUG 22, 2018
Recalling firm:
Tyson Foods Discovery Center
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled May 18, 2018

Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz plastic bag. 833-AVL-KRTM www.piouslion.com

The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.

Full report

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

Recall #:
F-1546-2018
Lot/product code:
There are no codes on the product.
Recalling firm:
Pious Lion
View official FDA record (opens in a new tab)