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 48,132 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported Apr 8, 2020
Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 Excimer Laser System is designed to treat the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Philips V60 Ventilators with Power Management PCBA part number 1055906
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
FDA (openFDA device enforcement)
Reported Apr 8, 2020
NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusable instrument designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2020
C-Reactive Protein Kit for use on the SPAplus, REF NK044.S.A, Rx only, UDI (01)05051700018456,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Gentamicin 80mg/60 mL Irrigation, containers, The Medicine Shoppe, 3524 B Tamiami Trail Port Charlotte, FL 33952
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Medicine Shoppe Pharmacy
FDA (openFDA drug enforcement)
Reported Apr 8, 2020
HUANGFUSHANZHEN; Dried Mushroom; Net Weight: 170G/6 OZ; Ingredient: Dried Mushroom; PRODUCT OF CHINA; SOLE AGENT:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tiffany Food Corp.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical, LLC
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diabetes Care, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
LN 3R70-01; software version 2.6.2 and earlier. The software is used with the Alinity i (LN 03R65-01) processing module…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Apr 1, 2020
American Classic Snack Company Sweet Bourbon Crunchers Pretzels in 8 oz. bags, 12 bags per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Classic Snack Co., LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2020
1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Enoki Mushroom; Product of Korea; Net Wt. 7.05 oz., (200 g) UPC: 7 426852 625810 The Enoki is packaged in a clear film,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hong Bin Foods LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Clover seed in 50 lb. woven poly bags, 40 bags to a pallet.
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holding Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Buprexone Banana cream 6-0.6 mg Troche, supplied in plastic troche molds with cardboard outer sleeve, Thrive Pharmacy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Matthew 7:25 Inc. dba Thrive Pharmacy
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 1, 2020
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Cardiovascular Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Southern Sisters Gourmet Apple Crisp mix
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southern Sisters Gourmet
7 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 25, 2020
Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2020
AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa N.V.
FDA (openFDA device enforcement)
Reported Mar 25, 2020
CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CME America, LLC
FDA (openFDA device 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.