The Recall Desk

State

Florida product recalls

72,907 recalls have nationwide distribution and so reach Florida. 12,818 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,818
Critical
1,764
Severe
2,975
Most recent
2026-09-09

Of the 12,818 recalls naming Florida we have scored against our rubric, 1,764 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,975 (23%) are Severe.

These figures cover only the 12,818 recalls whose distribution notice names Florida specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1576–1600 of 85725

  • HighFDA (Devices)·Z-2308-2026·2026-06-10

    Stapes prosthesis pistons carry an incorrect functional length on labeling

    Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.

    Product
    TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2026·2026-06-10

    Aligned Medical fluids kits contain recalled lidocaine injection

    Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.

    Product
    Aligned Medical AMS16835 Fluids Kit RX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2290-2026·2026-06-10

    Philips Azurion 7M12 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0567-2026·2026-06-10

    Discount Drug Mart antacid tablets contain small metallic particles

    Discount Drug Mart Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    DISCOUNT drug mart, EXTRA STRENGTH, ANTACID TABLETS, Calcium Carbonate 750 mg, 96 Tablets, Distributed by: Drug Mart- Food Fair Medina, OH 44256, UPC: 0 93351 03992 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1030-2026·2026-06-10

    Chewie Susans thumbprint cookie snack platters do not declare pecan

    Albertsons store-made Platter Snack Chewie Susans Thumbprints is being recalled because the contains statement does not declare pecan. 158 units are affected.

    Product
    UPC 22304700000 PLATTER SNACK CHEWIE SUSANS THUMBPRINTS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1044-2026·2026-06-10

    Albertsons ready meals meatloaf does not declare anchovy allergen

    Albertsons store-made Ready Meals Meatloaf is being recalled because the contains statement does not declare anchovy. 353 units are affected.

    Product
    UPC 21409600000 READY MEALS MEATLOAF SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0893-2026·2026-06-10

    Straus Family Creamery vanilla bean ice cream may contain metal

    Straus Family Creamery Vanilla Bean Organic Super Premium Ice Cream in pints is being recalled over potential contamination with foreign objects, specifically metal pieces.

    Product
    STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100306
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-2262-2026·2026-06-10

    Baxter Exacta Mix inlet sets may contain incorrect 0.8-micron filters

    Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.

    Product
    Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2292-2026·2026-06-10

    Arvis Hip and Knee 3.0 trackers may show wear and corrosion

    Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.

    Product
    Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0896-2026·2026-06-10

    Straus Family Creamery Dutch chocolate ice cream may contain metal

    Straus Family Creamery Dutch Chocolate Organic Super Premium Ice Cream in quarts is being recalled over potential contamination with foreign objects, specifically metal pieces.

    Product
    STRAUS FAMILY CREAMERY Dutch Chocolate ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100122
    Category
    Food
    Distribution
    17 states
  • HighFDA (Food)·H-1032-2026·2026-06-10

    Albertsons pork meat pies do not declare anchovy allergen

    Albertsons store-made pork meat pies are being recalled because the contains statement does not declare anchovy. 790 units in total are affected.

    Product
    UPC 21176300000 MEAT PIE PORK 4CT SS COLD UPC 21025900000 PIE PORK FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0961-2026·2026-06-10

    Cakerie strawberry shortcake triangles do not declare hazelnut allergen

    Albertsons store-made Cake Cakerie Strawberry Shortcake Triangle is being recalled because the contains statement does not declare hazelnut. 71 units are affected.

    Product
    UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1024-2026·2026-06-10

    Albertsons pad thai chicken meal does not declare anchovy

    Albertsons store-made Wok Pad Thai Chicken with Egg Roll is being recalled because the contains statement does not declare anchovy. 12 units are affected.

    Product
    UPC 21379600000 Ready Meals WOK PAD THAI CHICKEN WITH EGG ROLL SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1073-2026·2026-06-10

    Albertsons berry and salmon salad omits salmon and walnut declarations

    Albertsons store-made Fresh Berry & Salmon Salad is being recalled because the contains statement does not declare salmon and walnut. 90 units are affected.

    Product
    UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1002-2026·2026-06-10

    Albertsons cilantro lime shrimp does not declare anchovy allergen

    Albertsons store-made Shrimp 41-50 P&D with Cilantro Lime Marinade is being recalled because the contains statement does not declare shrimp and anchovy.

    Product
    UPC 23168600000 SHRIMP 41-50 P&D With CILANTRO LIME MARINADE 5% This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0559-2026·2026-06-10

    Tums assorted fruit antacid tablets contain small metallic particles

    Haleon Tums Antacid Assorted Fruit Tablets, 750 mg, in 330-count bottles are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 750 mg, 330-count bottle, Haleon, Warren, NJ 07059, UPC 3 0766 3072 10 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2296-2026·2026-06-10

    Avanta administration tube sets may not engage the flow control valve

    Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.

    Product
    Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0565-2026·2026-06-10

    CareOne extra strength calcium antacid tablets contain metallic particles

    CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    EXTRA STRENGTH ANTACID — EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2306-2026·2026-06-10

    GE MAC 5 ECG systems may link data to the wrong patient

    GE MAC 5 A4 and A5 Resting ECG Analysis Systems are being recalled because a development software version was released that can associate clinical information with the wrong patient.

    Product
    MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0571-2026·2026-06-10

    Hy-Vee extra strength antacid tablets contain small metallic particles

    Hy-Vee Extra Strength Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1012-2026·2026-06-10

    Albertsons duo seafood salad with crackers does not declare whiting

    Albertsons store-made Ready Meals Duo Seafood Salad with Crackers is being recalled because the contains statement does not declare whiting. 286 units are affected.

    Product
    UPC 27183100000 Ready Meals DUO SEAFOOD SALAD W/CRACKERS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2302-2026·2026-06-10

    BD Pyxis MedStation fingerprint scanners may overheat and cause burns

    BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.

    Product
    BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2291-2026·2026-06-10

    Philips Azurion 7M20 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0992-2026·2026-06-10

    Albertsons elegant charcuterie tray does not declare pistachio allergen

    Albertsons store-made Tray Charcuterie Elegant is being recalled because the contains statement does not declare pistachio. Eight units are affected.

    Product
    UPC 29138800000 TRAY CHARCUTERIE ELEGANT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1037-2026·2026-06-10

    Albertsons turkey poppyseed salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Turkey Poppyseed is being recalled because the contains statement does not declare almond.

    Product
    UPC 29361000000 KITCHEN SALAD TURKEY POPPYSEED SS COLD UPC 29360900000 KITCHEN SALAD TURKEY POPPYSEED FS COLD This is Albertson's store-made item and sold by random at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide