State

Florida product recalls

73,100 recalls have nationwide distribution and so reach Florida. 12,854 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total: 12,854
Critical: 1,775
Severe: 2,990
Most recent: 2026-09-25

Of the 12,854 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 2,990 (23%) are Severe.

Which agencies issued them

These figures cover only the 12,854 recalls whose distribution notice names Florida specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9426–9450 of 85954

HighFDA (Devices)·Z-0640-2025·2024-12-11
MEDLINE convenience kits recalled due to defective component
Medline is recalling multiple lots of its convenience kits because they contain a component (SafeAir Smoke Evacuation Pencil) that was previously recalled by Stryker. The affected kits are distributed nationwide.
Product
MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK, REF CDS780202P; 2) BASIC NEURO PACK, REF CDS780202Q; 3) BASIC NEURO PACK, REF CDS780202R; 4) ACDF CDS, REF CDS941061M; 5) NEURO KIT, REF CDS981327Q; 6) ZALE V-P SHUNT CDS, REF CDS983186J; 7) NEURO PACK-LF, R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0076-2025·2024-12-11
Levothyroxine Sodium Tablets Recalled Due to Subpotency Nationwide
Accord Healthcare is recalling Levothyroxine Sodium 75 mcg tablets (Lot D2300191, expiring 12/31/2025) distributed nationwide due to subpotency. Affected patients should contact their healthcare provider.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0080-2025·2024-12-11
Venofer Iron Sucrose Injection Recalled for Potential Glass Contamination
American Regent is recalling specific lots of Venofer (iron sucrose) injection due to potential glass delamination from vials. The affected drug is distributed nationwide.
Product
VENOFER — VENOFER (IRON SUCROSE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0236-2025·2024-12-11
Fruit Punch Recalled Due to Metal Fragment Contamination Risk
Sysco Fruit Punch 24-ounce products are recalled due to metal fragments introduced during dextrose production. Consumers should not consume the affected product and contact their retailer for refund or replacement.
Product
SYSCO FRUIT PUNCH, NET WT. 24OZ, Case UPC 10074865093221, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Drugs)·D-0109-2025·2024-12-11
Cinacalcet Tablets Recalled for Elevated Nitrosamine Impurity
AvKARE is recalling 2,396 bottles of Cinacalcet Tablets 60 mg (Lot #44550) distributed nationwide due to CGMP deviations. The tablets contain N-Nitroso-Cinacalcet, a nitrosamine impurity, above acceptable intake limits.
Product
Cinacalcet Tablets, 60 mg, 30-count bottle, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 42291-460-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0593-2025·2024-12-11
BD BACTEC FX Instrument Top credential compromise enables unauthorized access risk
BD service credentials for BACTEC FX instruments were accessed by an unauthorized actor, creating risk of unauthorized system access until credentials are updated.
Product
BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Number: 441385
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0592-2025·2024-12-11
BD Phoenix M50 Automated Microbiology System Service Credentials Exposed
BD confirmed that service credentials used by technical support teams were accessed by an unauthorized actor, creating a risk of unauthorized access to BD microbiology systems and associated data.
Product
BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catalog Number: 443624
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0221-2025·2024-12-11
Multivitamin supplement recalled for undeclared drugs and aspartame
Armonia Natural Store LLC is recalling OneMultivitaminic GAF-PLUS Advance 300ml for containing undeclared Acetaminophen, Dexamethasone Phosphate, and Aspartame. Consumers should discontinue use immediately.
Product
OneMultivitaminic GAF-PLUS Advance 300ml, plastic bottle, Room Temperature
Category
Drug
Distribution
12 states
HighFDA (Food)·F-0239-2025·2024-12-11
SYSCO Vanilla Instant recalled due to metal fragments in product
SYSCO Vanilla Instant (24oz pouches, Lot 268 ECA) is recalled because a damaged sifter introduced metal fragments into the product. Consumers should not consume affected products.
Product
SYSCO VANILLA INSTANT, NET WT. 24OZ, Case UPC 10074865103791, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Food)·F-0237-2025·2024-12-11
Sysco Low Cal Lemonade Recalled for Metal Fragments
DYMA Brands is recalling Sysco Low Cal Lemonade (8.6 oz pouches) due to metal fragments introduced during production. The product was distributed across 29 states.
Product
SYSCO LOW CAL LEMONADE, NET WT. 8.6OZ, Case UPC 00734730132648, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Food)·F-0222-2025·2024-12-11
AROMA VITA Hot Cocoa Mix Recalled for Metal Fragments
AROMA VITA Hot Cocoa Mix is being recalled due to metal fragments in the product caused by a damaged sifter used during dextrose production.
Product
AROMA VITA HOT COCOA MIX, NET WT. 32OZ (2LBS) 907g, UPC 7 1908 50007 0, Case UPC 50719098500075, Distributed by DYMA Brands, Inc. Atlanta, GA 30328
Category
Food
Distribution
30 states
HighFDA (Food)·F-0240-2025·2024-12-11
THIRSTER Lemonade Drink Mix Recalled for Metal Fragment Contamination
DYMA Brands recalls THIRSTER Lemonade Drink Mix because a damaged sifter used in dextrose production introduced metal fragments into the product. The product was distributed to 29 states.
Product
THIRSTER Lemonade Drink Mix NATURALLY FLAVORED LOW CALORIE, NET WT. 8.6 OZ (244 g), UPC 7 58108 39736 4, Case UPC 50758108397359, DISTRIBUTED BY US FOODS, INC. ROSEMONT, IL 60018
Category
Food
Distribution
30 states
HighFDA (Drugs)·D-0089-2025·2024-12-11
Array Liquid Antiseptic Handwash Recalled for Microbiological Test Failures
Midlab Incorporated is recalling Array Liquid Antiseptic Handwash due to manufacturing quality deviations. The product failed microbiological testing and may not provide adequate antimicrobial protection.
Product
Array Liquid Antiseptic Handwash, Chloroxylenol 0.1%, NET CONTENTS: 128 FL OZ (1 GAL) 3.785 L, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0598-2025·2024-12-11
Cartiva Synthetic Cartilage Implants Recalled Due to Higher Complication Rates
Cartiva Synthetic Cartilage Implants are being recalled due to higher-than-expected rates of complications including implant displacement, subsidence, nerve damage, and fragmentation. Patients with these implants should consult their surgeon.
Product
Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0250-2025·2024-12-11
Cinnamon Apple Cider Recalled for Elevated Patulin Contamination
Apple Wedge Cinnamon Apple Cider is being recalled due to elevated patulin contamination detected in testing. Affected products were distributed to Georgia, North Carolina, South Carolina, and Florida.
Product
Cinnamon Pasteurized APPLE WEDGE CIDER 1/2 Gal. (1.89L) HENDERSONVILLE, NC 28792 Keep Refrigerated Produce of USA Ingredients: Apples, Natural Cinnamon Flavor. 0.1% Potassium Sorbate Added as Preservative UPC 0 36482 64002 1
Category
Food
Distribution
4 states
HighFDA (Drugs)·D-0098-2025·2024-12-11
Diltiazem Hydrochloride Capsules Recalled Due to Nitrosamine Impurity
Glenmark Pharmaceuticals is recalling Diltiazem Hydrochloride capsules because they contain a chemical impurity above safe limits. About 7,296 bottles were distributed nationwide.
Product
DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0235-2025·2024-12-11
Vanilla Pudding Mix Recalled Due to Metal Fragment Contamination
Sysco Classic Vanilla Instant Pudding & Pie Filling Mix is recalled for metal fragments found in the product due to a damaged sifter used during dextrose production.
Product
Sysco Classic Vanilla Instant Pudding & Pie Filling Mix Natural and Artificial Flavor, NET WT. 32 OZ (2 LB) 907g, UPC 0 74865 20116 2, Case UPC 10074865201169, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Devices)·Z-0595-2025·2024-12-11
BACTEC 9120 System Recalled Due to Compromised Service Credentials
BD recalled BACTEC 9120 Systems because technical support credentials were compromised by an unauthorized actor. Until credentials are updated, there is a risk of unauthorized access to the devices and associated data.
Product
BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0234-2025·2024-12-11
Sysco Classic Strawberry Drink Mix recalled for metal fragment contamination
Sysco Classic Strawberry Drink Mix is being recalled due to metal fragments discovered during production. A damaged sifter in dextrose processing introduced the contamination into the product.
Product
Sysco Classic Strawberry Drink Mix Artificial Flavor, NET WT. 24OZ (1 LB 8 OZ) 690g, UPC 0 74865 09328 6, Case UPC 10074865093283, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Food)·F-0227-2025·2024-12-11
Katy's KITCHEN Gelatin Mix Recalled for Metal Fragments
Katy's KITCHEN Originals gelatin mix products are being recalled because a damaged sifter introduced metal fragments during manufacturing. The affected flavors are Lemon, Lime, and Orange, distributed across 29 states.
Product
Katy's KITCHEN Originals LEMON GELATIN MIX MEXCLA DE GELATINA DE LIMON, NET WT. 24 OZ. (1.5 LBS.) 680 g, UPC 8 22486 11794 8, Case UPC 30822486117918; Katy's KITCHEN Originals LIME GELATIN MIX, NET WT. 24 OZ. (1.5 LBS.) 680 g, UPC 8 22486 11795 5 & Katy's KITCHEN Originals ORANGE
Category
Food
Distribution
30 states
HighFDA (Food)·F-0231-2025·2024-12-11
Sysco Fruit Punch Drink Mix recalled for metal fragments
Sysco Classic Fruit Punch Drink Mix is being recalled due to metal fragments introduced by a damaged sifter during manufacturing. The affected product (Case UPC 00734730132709, Lot 263 EFA) was distributed across 29 states.
Product
Sysco Classic Fruit Punch Drink Mix Natural and Artificial Flavor, NET WT. 8.6OZ (244 G), Case UPC 00734730132709, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
Category
Food
Distribution
30 states
HighFDA (Drugs)·D-0079-2025·2024-12-11
Cinacalcet Tablets Recalled for N-Nitroso Impurity Exceeding FDA Safety Limit
Aurobindo Pharma USA recalls Cinacalcet 90 mg tablets nationwide due to N-nitroso impurity exceeding FDA's interim safety limit. The impurity is a known carcinogenic compound.
Product
Cinacalcet Tablets, 90 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-833-30), b) 500-count HDPE bottle (NDC 65862-833-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India. 90 mg - 30 Tablets - NDC 658
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0241-2025·2024-12-11
Thirster Low Cal Fruit Recalled for Metal Fragment Contamination
Dyma Brands recalls Thirster Low Cal Fruit due to metal fragments in the product from a damaged sifter during dextrose production. The affected pouches were distributed across 29 states.
Product
THIRSTER LOW CAL FRUIT, NET WT. 8.6OZ, Case UPC 50758108397380, DISTRIBUTED BY US FOODS, INC. ROSEMONT, IL 60018
Category
Food
Distribution
30 states
HighFDA (Devices)·Z-0585-2025·2024-12-11
BD EpiCenter Data Management System Credential Compromise Poses Unauthorized Access Risk
Service credentials for the BD EpiCenter Data Management System were accessed by an unauthorized actor. Until credentials are updated, system data and access controls are at risk.
Product
BD EpiCenter Data Management System Version or Model: 440887 Catalog Number: 440887
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0081-2025·2024-12-11
Iron sucrose injection recall due to potential glass contamination in vials
VENOFER (iron sucrose) injection is being recalled nationwide because certain vials may contain glass particles from potential glass delamination. Patients and healthcare providers should contact their pharmacist or healthcare provider immediately.
Product
VENOFER — VENOFER (IRON SUCROSE)
Category
Drug
Distribution
Distributed nationwide