State

Florida product recalls

73,219 recalls have nationwide distribution and so reach Florida. 12,856 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total: 12,856
Critical: 1,775
Severe: 2,991
Most recent: 2026-10-06

Of the 12,856 recalls naming Florida we have scored against our rubric, 1,775 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,991 (23%) are Severe.

Which agencies issued them

These figures cover only the 12,856 recalls whose distribution notice names Florida specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16101–16125 of 86075

SevereFDA (Food)·F-1494-2023·2023-09-20
Zespri Organic Green Kiwi recalled for Listeria monocytogenes contamination
Zespri Organic Green Kiwi from New Zealand is being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed across 14 states.
Product
Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 1lb. UPC 818849020093. Distributed by The Oppenheimer Group, 180 Nickerson Street, Suite 211 Seattle WA. Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged…
Category
Food
Distribution
14 states
SevereFDA (Devices)·Z-2506-2023·2023-09-20
Proclaim XR 7 Implantable Pulse Generators unable to exit MRI mode
Abbott Medical is recalling Proclaim XR 7 Implantable Pulse Generators due to a malfunction that prevents patients from exiting MRI (Magnetic Resonance Imaging) mode, potentially disrupting normal device operation and therapy delivery.
Product
Proclaim" XR 7 Implantable Pulse Generator REF 3662 (previously known as Proclaim" 7 Elite IPG) Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2508-2023·2023-09-20
Proclaim Plus 7 Implantable Pulse Generator Cannot Exit MRI Mode
Abbott Medical recalled Proclaim Plus 7 Implantable Pulse Generators due to a defect preventing patients from exiting MRI mode. This operational failure could compromise device functionality during or after magnetic resonance imaging procedures.
Product
Proclaim Plus 7 Implantable Pulse Generator REF 3672 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1495-2023·2023-09-20
Zespri Organic Green Kiwi Recalled Due to Listeria Contamination
Zespri Organic Green Kiwi from New Zealand has been recalled due to potential Listeria monocytogenes contamination. The recalled pallet was distributed across 14 U.S. states.
Product
Zespri Organic Green Kiwi, product of New Zealand, one pallet of bulk loose organic green kiwifruit was shipped to one consignee in Chicago, IL. The master carton has the barcode 067834 and the kiwi PLU label has the code GTIN 9400 9552.
Category
Food
Distribution
14 states
SevereFDA (Devices)·Z-2511-2023·2023-09-20
Infinity 7 Implantable Pulse Generator Recall Due to MRI Mode Exit Failure
Abbott Medical recalls Infinity 7 Implantable Pulse Generators due to reports that patients cannot exit MRI mode. The FDA has classified this as a Class I recall affecting devices distributed worldwide.
Product
Infinity 7 Implantable Pulse Generator REF 6662 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2507-2023·2023-09-20
Abbott Proclaim Plus 5 Implantable Pulse Generator MRI Mode Exit Failure
Abbott Medical is recalling Proclaim Plus 5 Implantable Pulse Generators (Model 3670) due to reports that patients are unable to exit MRI mode on the devices.
Product
Proclaim Plus 5 Implantable Pulse Generator REF 3670 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1180-2023·2023-09-20
WEFUN Capsules Recalled: Unapproved Drug with Undisclosed Sildenafil
WEFUN Capsules 825 mg are being recalled due to contamination with sildenafil, an undisclosed active pharmaceutical ingredient not approved for the product. Distribution was nationwide.
Product
WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2505-2023·2023-09-20
Proclaim XR 5 Implantable Pulse Generators Cannot Exit MRI Mode
Abbott Medical recalled the Proclaim XR 5 Implantable Pulse Generator after patients reported being unable to exit MRI mode on their devices. Approximately 113,784 units were distributed worldwide.
Product
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1148-2023·2023-09-20
Pantoprazole Sodium for Injection Recalled Due to Sterility Concern
BE Pharmaceuticals is recalling Pantoprazole Sodium for Injection nationwide due to lack of sterility assurance caused by powder discoloration and small cracks in some vials. No illnesses have been reported.
Product
PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1516-2023·2023-09-20
Knorr Alphabet Pasta Soup Recalled for Undeclared Egg Allergen
Knorr Letras con Tomate soup mix is being recalled because it contains undeclared egg. Consumers with egg allergies should not consume this product.
Product
Knorr Letras con Tomate Tomato Based Alphabet Pasta Soup Mix 3.5 oz UPC: 048001716186
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2582-2023·2023-09-20
ACUSON Redwood 2.0 Ultrasound Systems Display Incorrect Measurement Results
ACUSON Redwood 2.0 ultrasound systems may display underestimated measurement results when using an 18L6 transducer in Dual format, potentially leading to patient misdiagnosis. 796 units are affected worldwide.
Product
ACUSON Redwood 2.0 ultrasound systems, REF: 11503314
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1508-2023·2023-09-20
Trader Joe's Almond Windmill Cookies Recall: Rocks Found in Product
Fantasy Cookie Corporation is recalling Trader Joe's Almond Windmill Cookies because rocks were found in the product. Consumers should not eat affected cookies.
Product
Trader Joe's Almond Windmill Cookies Buttery, tender cookies topped with crunchy almonds. Net Wt. 15 oz.
Category
Food
Distribution
8 states
HighFDA (Food)·F-1514-2023·2023-09-20
Knorr Pasta Soup Mix recalled for undeclared egg allergen
Conopco (Unilever) recalled Knorr Estrellitas con Tomate soup mix nationwide due to undeclared egg allergen. No illnesses have been reported.
Product
Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix 3.5 oz UPC: 048001716193
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2588-2023·2023-09-20
FILMARRAY GI Panel Software Recalled for False Positive Cryptosporidium Results
BioFire Diagnostics is recalling FILMARRAY Gastrointestinal Panel software due to an increased risk of false positive Cryptosporidium test results. Approximately 61,069 devices were distributed in the US and internationally.
Product
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Category
Medical Device
Distribution
54 states
HighFDA (Devices)·Z-2524-2023·2023-09-20
Medtronic Bone Graft Recalled Due to Incorrect Size Labeling
Medtronic Sofamor Danek USA Inc is recalling Magnifuse Bone Graft products due to incorrect size labeling on 55 pouches. Units with specific serial numbers were distributed in nine U.S. states.
Product
Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V643000·2023-09-20
Tiffin motorhomes recalled for cooktop electrical shock hazard
Tiffin is recalling certain 2016-2024 Allegro Bus and 2017-2024 Zephyr motorhomes because the 240-volt cooktop may not be grounded, creating an electrical shock hazard. Tiffin will install a ground for the junction box at no charge.
Product
TIFFIN — TIFFIN ALLEGRO BUS, ZEPHYR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V674000·2023-09-20
GM Recalls 2014 Buick Verano and Chevrolet Cruze for Air Bag Defect
General Motors is recalling 2014 Buick Verano and Chevrolet Cruze vehicles because side roof-rail air bag inflators may rupture, potentially causing injury from metal fragments.
Product
CHEVROLET — CHEVROLET, BUICK CRUZE, VERANO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1505-2023·2023-09-20
Twin City Foods Frozen Corn Recalled for Listeria Contamination Risk
Multiple frozen corn products distributed nationwide are being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Product
Kernel Corn, BEST PRICE TOPVALU, net wt. per bag 300g. Label is in foreign language. UPC 4549414086232 Signature Select Golden Corn Super Sweet, Product of USA, net wt. per bag 12oz, 12 bags per case. UPC 21130090655 Food Lion Super Sweet Cut Yellow Corn, Product of USA, net…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·23V644000·2023-09-20
BMW Recalls 2023 740i, 760i, and i7 Models for Wiper Failure
BMW is recalling 2023 740i, 760i, and i7 vehicles because windshield wipers may fail in certain weather, reducing visibility and increasing crash risk.
Product
BMW — BMW 760I, I7, 740I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1515-2023·2023-09-20
Knorr Soup Mix Recalled for Undeclared Egg Allergen
Conopco is recalling Knorr Fideos con Tomate Tomato Based Pasta Soup Mix because it contains undeclared egg. The product was distributed nationwide with best-by dates through July 6, 2024.
Product
Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz UPC: 048001716162
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2578-2023·2023-09-20
Medical Device Recall: ACL TOP Coagulation Analyzers for Sample Misidentification
Instrumentation Laboratory is recalling ACL TOP coagulation analyzers due to potential sample misidentification that could result in incorrect test results and alter patient management decisions.
Product
ACL TOP Family 50 Series Models as follows: In vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis (1) ACL TOP 550 CTS Model…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V646000·2023-09-20
Wabash National Dry Van Trailers Recalled for Rear Impact Guard Defect
Wabash National is recalling certain 2009-2024 dry van trailers because the rear impact guard is positioned too far forward, potentially reducing crash protection. Dealers will add an extension to the guard free of charge.
Product
WABASH NATIONAL — WABASH NATIONAL VAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2531-2023·2023-09-20
Remel Todd Hewitt Broth Culture Medium May Fail to Detect Target Organism
One lot of Remel Todd Hewitt Broth culture medium may fail to recover Group B Streptococci during testing or use with patient samples, potentially resulting in missed diagnoses.
Product
remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containing mixed bacterial flora
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1509-2023·2023-09-20
Trader Joe's Dark Chocolate Chunk and Almond Cookies Recalled for Rock Contamination
Trader Joe's Dark Chocolate Chunk and Almond Cookies are being recalled due to contamination with rocks. Approximately 110,088 units were distributed to stores in Pennsylvania, Florida, California, Texas, Illinois, Washington, and Arizona.
Product
Trader Joe's Dark Chocolate Chunk and Almond Cookies Net Wt. 13 oz.
Category
Food
Distribution
8 states
HighFDA (Food)·F-1503-2023·2023-09-20
Twin City Foods Frozen Corn Recalled Nationwide for Listeria Risk
Twin City Foods recalled frozen corn products due to potential Listeria monocytogenes contamination. Products distributed nationwide and internationally.
Product
Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processing. Bulk tote labels have cooking instructions. Individually Quick Frozen (IQF) Super Sweet Corn, foodservice item, packaged in 32oz. plastic bag, 12 bags per…
Category
Food
Distribution
Distributed nationwide