Recalls distributed in Florida
These notices name Florida in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
6,421 stored notices name Florida, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported May 8, 2024
The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported May 8, 2024
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2024
3M Durapore Surgical Tape, Catalog Number 1538-118
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported May 1, 2024
Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported May 1, 2024
Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amy's Kitchen Inc.
FDA (openFDA food enforcement)
Reported May 1, 2024
Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 1, 2024
IBA Proton Therapy System - PROTEUS 235, PTS-10 versions, PTS-11 versions, and PTS-12 versions.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported May 1, 2024
Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Parker Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2024
QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2024
Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Route 92 Medical Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 1, 2024
Mariner RDX Polyaxial Head, REF: MX1-000020; Mariner RDX Extended Polyaxial Head, REF: MX1-000030; Mariner RDX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2024
ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 1, 2024
LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.XENEX Disinfection Services Inc.
FDA (openFDA device enforcement)
Reported May 1, 2024
NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2024
Aromitalia Malasia Coconut Paste + 35.27 oz milk-based mix, Net Weight 123.46 oz, plastic container.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aromitalia USA Inc.
FDA (openFDA food enforcement)
Reported Apr 24, 2024
Tranquility & Teachings William Monague plate set, brand Indigenous Collection by CAP. Each box consists of two plates,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canadian Art Prints
FDA (openFDA food enforcement)
Reported Apr 24, 2024
Identity Imprint PS Tibial Tray Size 4: Lot 540287
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conformis, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2024
ConSup North America Inc. Recalls Ready-To-Eat Sliced Prosciutto Product Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.ConSup North America Inc.
USDA FSIS
Reported Apr 24, 2024
Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Masimo Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2024
Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001
High riskUsing this product could cause serious injury, illness or death — stop using it now.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2024
AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
High riskUsing this product could cause serious injury, illness or death — stop using it now.SonarMed Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2024
Neria Soft Infusion Set, Product Code 507302, intravascular administration set
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unomedical A/S
FDA (openFDA device enforcement)
Reported Apr 17, 2024
Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2024
SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 retail units per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raja Foods LLC
FDA (openFDA food enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.