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.

Which agencies issued them

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.

1526–1550 of 85725

HighFDA (Devices)·Z-2293-2026·2026-06-10
Arvis Hip and Knee 2.0 trackers may show wear and corrosion
Arvis Hip & Knee 2.0 Instrument Sets are being recalled because the Impactor V-Block Assembly and Trackers may show early wear or corrosion on the exposed magnet face.
Product
Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2026·2026-06-10
BD Pyxis Anesthesia Station fingerprint scanner may overheat and burn
The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.
Product
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2300-2026·2026-06-10
BD Pyxis Anesthesia Station 4000 fingerprint scanner may overheat
The BD Pyxis Anesthesia Station 4000 is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0994-2026·2026-06-10
Albertsons Twisted Bliss pretzel trays do not declare almond allergen
Albertsons store-made Twisted Bliss Pretzel Tray is being recalled because the contains statement does not declare almond. Two units are affected.
Product
UPC 29344500000 TWISTED BLISS PRETZEL TRAY 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-1000-2026·2026-06-10
Albertsons shrimp and surimi ceviche does not declare sea bream
Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.
Product
UPC 23245700000 SHRIMP & SURIMI CEVICHE FRESH 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 (Devices)·Z-2298-2026·2026-06-10
BD Pyxis MedStation ES fingerprint scanner may overheat and burn
The BD Pyxis MedStation ES medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedStation ES REF: 323 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1018-2026·2026-06-10
Albertsons caesar salads do not declare anchovy allergen
Albertsons store-made Kitchen Caesar Salads in large and small sizes are being recalled because the contains statement does not declare anchovy. 39 units are affected.
Product
UPC 29787600000 Kitchen SALAD CAESAR LARGE SS COLD UPC 21543200000 Kitchen SALAD CAESAR SMALL 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 (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 (Drugs)·D-0570-2026·2026-06-10
Harris Teeter ultra strength antacid tablets contain metallic particles
Harris Teeter Ultra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
Harris Teeter, ULTRA STRENGTH ANTACID, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, Distributed by: Harris Teeter, LLC.,MATTHEWS, NC 28105, UPC: 0 72036-73108-1.
Category
Drug
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-0556-2026·2026-06-10
Ascend amlodipine and olmesartan tablets failed dissolution specifications
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2297-2026·2026-06-10
BD Pyxis MedStation 4000 fingerprint scanner may overheat and burn
The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2282-2026·2026-06-10
Neptune docking station shipped without verified electrical safety testing
A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.
Product
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Category
Medical Device
Distribution
Distributed nationwide
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 (Food)·H-1017-2026·2026-06-10
Albertsons apple waldorf salad does not declare walnut allergen
Albertsons store-made Apple Waldorf Salad is being recalled because the contains statement does not declare walnut. 33 units are affected.
Product
UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WALDORF FS UPC 27169500000 Kitchen SALAD APPLE WALDORF LRG UPC 27170300000 Kitchen SALAD APPLE WALDORF MED UPC 27169300000 Kitchen SALAD APPLE W
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0970-2026·2026-06-10
Albertsons Mexican wedding cookies do not declare pecan allergen
Albertsons store-made Mexican Wedding Cookies, 8 count, are being recalled because the contains statement does not declare pecan. 445 units are affected.
Product
UPC 22358600000 COOKIES MEXICAN WEDDING 8 CT 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-2287-2026·2026-06-10
Philips Azurion 5M20 Roadmap Pro may produce unusable dark images
Philips Azurion 5M20 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 5M20, Model Numbers: 722228 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-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-2294-2026·2026-06-10
Digital angiography and radiography systems may remain energized when switched off
Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.
Product
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D15
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0905-2026·2026-06-10
Second Nature Keto Crunch mix may contain undeclared cashews and pistachios
Second Nature Keto Crunch Smart Mix is being recalled because the product may contain undeclared allergens, specifically cashews and pistachios, along with dried cherries.
Product
SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1022-2026·2026-06-10
Albertsons fresh berry and chicken salad does not declare walnut
Albertsons store-made Ready Meals Salad Fresh Berry & Chicken is being recalled because the contains statement does not declare walnut. 228 units are affected.
Product
UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN 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-0963-2026·2026-06-10
Albertsons raspberry moon cake does not declare almond allergen
Albertsons store-made Cake Raspberry Moon 8-inch 2-layer is being recalled because the contains statement does not declare almond. 25 units are affected.
Product
UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer. 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 (Drugs)·D-0558-2026·2026-06-10
Tums assorted fruit antacid tablets contain small metallic particles
Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.
Product
HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0897-2026·2026-06-10
Straus Family Creamery mint chip ice cream may contain metal pieces
Straus Family Creamery Mint Chip Organic Super Premium Ice Cream in pints is being recalled over potential contamination with foreign objects, specifically metal pieces.
Product
STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100504
Category
Food
Distribution
17 states
HighFDA (Food)·H-0962-2026·2026-06-10
Chocolate lady madeleine strawberry cakes do not declare almond allergen
Albertsons store-made Cake Pav Chocolate Lady Madeleines Strawberry is being recalled because the contains statement does not declare almond. Six units are affected.
Product
UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry. 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