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Recalls affecting Florida

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

17,356 recalls found

Just announced

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

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 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
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
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

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
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, 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

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

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

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

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
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

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 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 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 June 19, 2018

DRY ROASTED MEDIUM CHOP PEANUT GRANULES NET WT 30LBS (13.61 KGS) Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332

The firm was notified by their customer that the product test positive for Salmonella

Full report

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

Recall #:
F-1652-2018
Lot/product code:
LOT# G-18151 JULIAN DATE: 18151 & LOT #G-18158 JULIAN DATE 18158
Recalling firm:
Peanut Processors, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled June 19, 2018

DRY ROASTED PEANUT MEAL NET WT 30LBS Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332

The firm was notified by their customer that the product test positive for Salmonella

Full report

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

Recall #:
F-1653-2018
Lot/product code:
ITEM# 2180 LOT# G-18151 PO# PL3-402521 JULIAN DATE 18151
Recalling firm:
Peanut Processors, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 15, 2018

Montelukast Sodium Tablets 10 mg, 30-count bottle, Rx Only, By: Hetero Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, Manfuactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, NDC 31722-726-30

Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg tablets may contain 90 tablets of Losartan Potassium 50 mg.

ALL 50 STATES
Full report

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

Recall #:
D-0081-2019
Lot/product code:
Lot #: MON17384, Exp 12/19
Recalling firm:
Hetero Labs Limited Unit V
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 4, 2018

Callie's Charleston Biscuits COUTRY HAM BISCUITS; 18 NET WT. 18 OZ (510 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM

The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes

Full report

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

Recall #:
F-0067-2019
Lot/product code:
050417, 052417, 053017, 071017, 072417, 080117, 081417, 082217, 091417, 092717, 101017, 101117, 102417, 110617, 110817, 111417, 112017, 113017, 120817, 121117, 121417, 121817, 122217, 070219, 071519, 081319, 082619, 090819, 091519, 092619, 092719, 101019, 101619, 102319, 110119, 111119, 111419, 112919, 121319, 122119, 010920, 013020, 020620 & 031920.
Recalling firm:
Callie's Charleston Biscuits
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 4, 2018

Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM

The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes

Full report

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

Recall #:
F-0066-2019
Lot/product code:
050417, 060617, 060717, 080117, 091917, 092717, 110617, 120417, 121617, 070619, 080819, 101019, 102319, 110119, 111419, 122119 & 010920.
Recalling firm:
Callie's Charleston Biscuits
View official FDA record (opens in a new tab)