State

Florida product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4676–4700 of 85758

HighFDA (Devices)·Z-0502-2026·2025-11-19
Second control serum lot recalled over negative HBsAg analyte recovery
Techno-Path is recalling 51 units of Multichem ID-B positive control serum from a second lot because of potential negative recovery of the HBsAg analyte on the Alinity i platform.
Product
Multichem ID-B. Model Number: SR103B. Intended for use as an unassayed positive qualitative quality control serum to monitor the precision of laboratory testing procedures for the determination of anti-HIV-1 IgG, anti-HBc IgG, anti-HTLV-I IgG, anti-HCV IgG, HBs antigen and ant
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-0483-2026·2025-11-19
Fifteen millimetre snares recalled over holes compromising package sterility
Olympus is recalling 18,174 Single Use Electrosurgical Snares SD-400U-15 because sterility may be compromised by small holes formed during packaging or transportation.
Product
Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0470-2026·2025-11-19
Small jaw sealers recalled over residual material that may dislodge
Medline is recalling 18,117 reprocessed LigaSure Small Jaw instruments because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0209-2026·2025-11-19
California rolls recalled over wheat and soy missing from allergen statement
Hana Group is recalling 373 packages of Mai California Roll because wheat and soy are missing from the product's Contains statement.
Product
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lid
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-0490-2026·2025-11-19
Reprocessed ultrasonic shears recalled because they may stick in the on position
Stryker Sustainability Solutions is recalling 22,476 reprocessed HARMONIC FOCUS shears because a manufacturing issue may leave them stuck in the on position, causing continuous activation.
Product
HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2026·2025-11-19
Maryland jaw sealers 23 cm recalled over residual material inside the device
Medline is recalling 4,007 reprocessed LigaSure Maryland Jaw sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2026·2025-11-19
Larger bore nasal feeding tubes recalled for possible occlusion
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 55 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0469-2026·2025-11-19
Impact vessel sealers recalled over residual material that may dislodge
Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Product
Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0455-2026·2025-11-19
Bedside patient monitors recalled over batteries that fail as backup power
GE Healthcare is recalling 7,408 B105P, B125P, B105M, B125M and B155M patient monitors because certain batteries can lose the ability to hold charge, causing a loss of monitoring.
Product
B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160001-065 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms 3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2026·2025-11-19
Maryland jaw sealers 44 cm recalled over trapped residual material
Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0498-2026·2025-11-19
Long nasal feeding tubes recalled from one lot for possible occlusion
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2026·2025-11-19
VATS lobectomy stapler boxes recalled over a malformed cover tube press
Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.
Product
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0496-2026·2025-11-19
Ninety centimetre nasal feeding tubes recalled for possible occlusion
Applied Medical Technology is recalling NutraGlide 5 F-6 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0495-2026·2025-11-19
Nasal feeding tubes recalled from one lot because they may be occluded
Applied Medical Technology is recalling NutraGlide 5 F-6 F x 55 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2026·2025-11-19
Mobile X-ray systems recalled over bolts that may loosen or fracture
NeuroLogica is recalling 236 GM85 digital mobile X-ray systems because the four M5 bolts securing the tube head unit to the arm may loosen or fracture from metal fatigue.
Product
GM85 Digital Mobile X-ray imaging System; Model Number: GM85;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0492-2026·2025-11-19
Allergy IgE universal kits recalled over barcodes misordering tubes in wedges
Siemens Healthcare Diagnostics is recalling 2,802 units of the 3gAllergy Specific IgE Universal Kit because barcode orientation causes the instrument to misread tube positions.
Product
3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UNS1), 3gAllergy Specific IgE Control Antibody (L2UNS2); Siemens Material Number (SMN): 10380875; Catalog Number: L2KUN6;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V800000·2025-11-19
McNeilus Recalls 2024-2025 Volterra ZSL Trucks Due to Software Error
McNeilus is recalling 2024-2025 Volterra ZSL side loader garbage trucks because a software error may cause grabber fingers to move without operator input, posing a risk of injury or crash.
Product
MCNEILUS — MCNEILUS VOLTERRA ZSL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0457-2026·2025-11-19
Monitor batteries recalled because they can lose the ability to charge
GE Healthcare is recalling 2,857 FLEX-3S2P lithium-ion batteries used with patient monitors because they can lose the capability to hold charge and provide backup power.
Product
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0499-2026·2025-11-19
Ceiling X-ray tube supports recalled over a shaft that may break
Shimadzu is recalling 1,766 ceiling type X-ray tube supports, models CH-200 and CH-200M, because the mounting shaft may break and the tube assembly could come off.
Product
Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The ceiling type x-ray tube support CH-200 is used to hold the X-ray tube and collimator to position the X-ray tube unit. This unit is used for radiographic ex
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0467-2026·2025-11-19
LigaSure Exact dissectors recalled over residual material that may dislodge
Medline is recalling 4,226 reprocessed LigaSure Exact dissectors, 21 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Exact, Dissector without Nano-Coating 21cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical Cutting And Coagulation Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2026·2025-11-19
Blunt tip sealers 44 cm recalled over trapped residual material
Medline is recalling 1,446 reprocessed LigaSure Blunt Tip sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 44cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2026·2025-11-19
Reprocessed vessel sealers recalled over residual material that may dislodge
Medline is recalling 57,244 reprocessed LigaSure Maryland Jaw sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Product
Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0482-2026·2025-11-19
Electrosurgical snares recalled over small holes compromising package sterility
Olympus is recalling 48,208 Single Use Electrosurgical Snares SD-400 because sterility may be compromised by small holes formed during packaging or transportation.
Product
Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of di
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0465-2026·2025-11-19
DigitalDiagnost C90 systems recalled over ceiling carriages resisting vertical movement
Philips is recalling 223 DigitalDiagnost C90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0500-2026·2025-11-19
Platelet reactivity tests recalled after an uncleared device was distributed
Accriva Diagnostics is recalling 125 boxes, 3,125 tests, of VerifyNow PRUTest because a device without premarket clearance was incorrectly packaged and distributed.
Product
VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.
Category
Medical Device
Distribution
Distributed nationwide