State

Florida product recalls

72,913 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 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2026–2050 of 85731

SevereFDA (Food)·H-0693-2026·2026-05-13
Griffith Goods milk and egg mix recalled over potential Salmonella contamination
Milk-N-Egg Mix in 50 lb bags is being recalled after the firm was notified by its supplier that the nonfat dry milk may be contaminated with Salmonella. 833 bags are affected.
Product
MILK-N-EGG MIX NET WEIGHT: 50 LBS, PROCESSED FROM NONFAT DRIED MILK, DRIED WHEY, DRIED EGG WHITES CONTAINS: EGG, MILK Mfred By: Griffith Goods, One Griffith Way, Stonecrest, GA
Category
Food
Distribution
15 states
SevereFDA (Drugs)·D-0518-2026·2026-05-13
BD PurPrep Povidone-Iodine Topical Solution Sterility Assurance Recall
CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.
Product
PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0513-2026·2026-05-13
DELFLEX Peritoneal Dialysis Solution Recall Due to Potential Sterility Issues
Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from bag perforations that could compromise sterility. Affected patients should contact their healthcare provider immediately.
Product
DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2.5% DEX. LM/LC, 2L 5PK, Part Number 054-20222, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1978-2026·2026-05-13
Halyard SAMMC Angiography Kit syringe rotating adapter unwinding recall
Halyard SAMMC ANGIOGRAPHY kits (Model SAMM066-15) are recalled because the Medline syringe rotating adapter may unwind during use, causing a loose or disconnected connection between the syringe and manifold. 2,392 kits were distributed across US states including FL, IL, MO, MS, NC, NE, and TX.
Product
Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
Category
Medical Device
Distribution
7 states
SevereFDA (Drugs)·D-0517-2026·2026-05-13
PurPrep Povidone-Iodine and Isopropyl Alcohol Solution Recalled for Sterility Assurance
CareFusion 213, LLC is recalling PurPrep sterile topical solution due to lack of assurance of sterility and potential product contamination. The affected product is a povidone-iodine and isopropyl alcohol solution distributed nationwide.
Product
PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0765-2026·2026-05-13
Raw Farm bulk shredded cheddar linked to multistate E. coli outbreak
Raw Farm Shredded Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Product
RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194
Category
Food
Distribution
10 states
SevereFDA (Drugs)·D-0540-2026·2026-05-13
Lactated Ringers Injection Recalled for Particulate Matter Contamination
B. Braun Medical Inc. is recalling Lactated Ringer's Injection USP (1000 mL containers) due to the presence of particulate matter. The recall affects 95,412 containers distributed nationwide.
Product
LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1936-2026·2026-05-13
Beacon Tip Centimeter Sizing Catheter recalled for cracking marker bands
Cook Incorporated is recalling Beacon Tip Centimeter Sizing Catheters because marker bands may crack or break, which could lead to device fragmentation, prolonged procedures, vessel injury, and in worst-case scenarios, life-threatening harm or death.
Product
Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 NR5.0-35-100-P-10S-0-CSC-20 G31214 NR5.0-35-100-P-10S-PIG-CSC-20 G31216 NR5.0-35-70-P-10S-VCF-CSC-20 G31220 NR5.0-35-100-P-10S-VCF-CSC-20 G31221 Sizing catheters are single-use, sterile
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0692-2026·2026-05-13
Chick-fil-A milk wash recalled over potential Salmonella contamination
Milk Wash packed exclusively for Chick-fil-A is being recalled after the firm's supplier reported that the nonfat dry milk may be contaminated with Salmonella.
Product
MILK WASH NET WEIGHT: 50OZ (1417g) Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, GA 30349
Category
Food
Distribution
15 states
SevereFDA (Devices)·Z-2097-2026·2026-05-13
Medline Convenience Kits recalled for potential sterilization issues
Medline Industries is recalling multiple convenience kit models due to calibration issues with equipment used to sterilize and package the devices, which could affect sterility assurance levels.
Product
See RES for full list. Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS, Model Number: CDS983069G; 2) CHP COCHLEAR SUPPLEMENT CDS, Model Number: CDS983069I; 3) HEAD & NECK CDS-LF, Model Number: CDS983782C; 4) BAPTIST FLOYD BRONCHOSCOPY, Model Number: DYKE1456D; 5) BRONCH
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1971-2026·2026-05-13
Halyard CARDIAC CATH PACK SAN23CARDQ Kit Syringe Adapter Risk
AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (Model DRCC36) due to a Medline syringe rotating adapter that may unwind during use, potentially causing loose or full disconnection between the syringe and manifold.
Product
Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Category
Medical Device
Distribution
7 states
SevereFDA (Devices)·Z-2062-2026·2026-05-13
ERBEFLO CleverCap CO2 Tubing and Cap Sets for Endoscopes
Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
Product
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Scopes & UCR, REF: 20325-240; Hybrid CO2 Tubing/Cap Set for Olympus Scopes, REF: 20325-206; Hybrid CO2 Tubing/Cap Set for Pentax Scopes, REF: 2
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1979-2026·2026-05-13
Halyard VA Detroit Cath Lab Pack Kit Syringe Adaptor Disconnection Risk
Halyard VA Detroit Cath Lab Pack kits (Model VMCD029) are being recalled due to a potential risk that the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Product
Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
Category
Medical Device
Distribution
7 states
SevereFDA (Drugs)·D-0519-2026·2026-05-13
Octreotide Acetate Injectable Suspension Recalled Due to Sterility Assurance
Teva Pharmaceuticals USA, Inc. is recalling 2,200 kits of Octreotide Acetate for Injectable Suspension (30 mg) due to quality system deficiencies that affect sterility assurance. The recall affects all lots nationwide.
Product
OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1973-2026·2026-05-13
Halyard CATH LAB Kit Recalled for Syringe Adapter Disconnection Risk
AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75AM) because the syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Product
Halyard CATH LAB kit. Model Number: SACL75AM.
Category
Medical Device
Distribution
7 states
SevereFDA (Devices)·Z-1970-2026·2026-05-13
Halyard Cardiac Cath Pack Kit Syringe Adapter Unwinding Risk
AVID Medical recalls Halyard Cardiac Cath Pack kits (Models EAMC1000-05, WAFB208-02) due to risk that a Medline syringe rotating adapter may unwind during use, causing loose or full disconnection between the syringe and manifold.
Product
Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
Category
Medical Device
Distribution
7 states
SevereFDA (Devices)·Z-1855-2026·2026-05-13
Intuitive 8 mm SureForm 30 Gray Reloads Incomplete Staple Defect
Intuitive Surgical is recalling Intuitive 8 mm SureForm 30 Gray Reloads (Reference Numbers 48230M-05 and 48230M-06) because they may produce an incomplete staple line during curved-tipped stapler operations.
Product
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
Category
Medical Device
Distribution
49 states
SevereFDA (Devices)·Z-1975-2026·2026-05-13
Halyard HEART CATH SELF REGIONAL kit syringe adapter disconnection hazard
AVID Medical is recalling the Halyard HEART CATH SELF REGIONAL kit (Model SELF131-05) because the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Product
Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
Category
Medical Device
Distribution
7 states
SevereFDA (Food)·H-0766-2026·2026-05-13
Raw Farm bulk raw cheddar linked to multistate E. coli outbreak
Raw Farm Original Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Product
RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160
Category
Food
Distribution
10 states
SevereFDA (Food)·H-0764-2026·2026-05-13
Raw Farm shredded raw cheddar linked to multistate E. coli outbreak
Raw Farm Raw Cheddar Simply Shredded Original in 8 oz packs is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Product
RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP REFRIGERATED INGREDIENTS: WHOLE RAW MILK, VEGETABLE RENNET, CULTURES, KOSHER SEA SALT Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 8
Category
Food
Distribution
10 states
SevereFDA (Devices)·Z-2106-2026·2026-05-13
Medline Convenience Kits recalled due to sterilization equipment calibration issues
Medline Industries is recalling four Convenience Kit models (892 units) nationwide because sterilization and packaging equipment calibration issues may have compromised the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY, Model Number: DYNDA2941A; 2) CHEST/BREAST-LF, Model Number: DYNJ83950; 3) HERNIA REPAIR TOTE, Model Number: DYNJ908337A; 4) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1972-2026·2026-05-13
Halyard Cardiac Catheterization Tray Kits Recalled for Connection Risk
AVID Medical is recalling Halyard CARDIAC CATH TRAY SHANDS JAX kits due to a defect in the Medline syringe rotating adaptor that may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Product
Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Category
Medical Device
Distribution
7 states
SevereFDA (Devices)·Z-1976-2026·2026-05-13
Halyard NEURO IR PERIPHERAL kit syringe adapter may disconnect
AVID Medical is recalling the Halyard NEURO IR PERIPHERAL (PS 64405) kit because the Medline syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Product
Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
Category
Medical Device
Distribution
7 states
SevereFDA (Devices)·Z-2091-2026·2026-05-13
Medline Convenience Kits Recalled for Sterilization Calibration Issues
Medline is recalling multiple convenience kits used in catheterization labs and surgical procedures due to calibration issues with sterilization equipment that may affect sterility assurance. The affected kits were distributed nationwide.
Product
Medline Convenience Kits: 1) ANGIO PROCEDURE PACK, Model Number:00-401824AA; 2) ENDO KIT W/SYRINGE, Model Number:DYKE1743; 3) BGMC ANGIOGRAPHY PACK-LF, Model Number:DYNJ0800934D; 4) GENERAL ENDO PACK-LF, Model Number:DYNJ0842873J; 5) ANGIO PROCEDURE PACK, Model Number:DY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2065-2026·2026-05-13
Physio-Control Defibrillators May Lack Required Performance Inspection
Physio-Control defibrillators (LIFEPAK 15, 1000, 35, and 20e models) serviced between July 2023 and November 2025 may not have undergone required Performance Inspection Procedures, potentially preventing therapy delivery.
Product
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958, 99577-001950, 99577-001962, 99577-002178, 99577-001372, 99577-00193
Category
Medical Device
Distribution
Distributed nationwide