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 48,122 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported May 5, 2021
Change Healthcare Enterprise Viewer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Canada Company
FDA (openFDA device enforcement)
Reported May 5, 2021
Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela AG Medical Technology
FDA (openFDA device enforcement)
Reported May 5, 2021
Power Wheelchair
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merits Holdings Co. dba Merits Health Products, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 5, 2021
Losartan Potassium USP, 50 mg, RX Only, Pkg By PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 60 Tablets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported May 5, 2021
CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Label - FaStep Rapid Diagnostic Test *** Rapid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Azure Biotech Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
The AMS 700 Inflatable Penile Prosthesis is a closed fluid-filled system containing saline. The system is made out of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Dawn Food Products, 7 2 Layer Vanilla Bean Waterfall Cake, 35 oz., cake is placed on a cardboard plate which is then…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rise Baking Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 28, 2021
BCS XP System: Multipurpose system for in vitro coagulation studies. Product code: 10459330, 10461894, 10470625 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
KeVita Cucumber Rosemary (primary package), 15.2 oz., glass bottles, 6 packages per case, refrigerated storage
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tropicana Products, Inc.
FDA (openFDA food enforcement)
Reported Apr 28, 2021
ELI 280 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn Inc. Mortara
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
VIDAS¿ CMV IgM 30 Tests
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
El Sembrador Peas and Carrots, poly bags, 12/16 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bonduelle USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 21, 2021
MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centinel Spine, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia stapling system. Staple…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Apr 21, 2021
HARRIS TEETER FRESH FOODS MARKET 3 Layer COOKIES & CREME CAKE NET WT 48 OZ (3 LB) 1.36kg packages PROUDLY DISTRIBUTED…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Harris Teeter
FDA (openFDA food enforcement)
Reported Apr 21, 2021
Disposable Sampling Tube, REF VSM01, Contents: Transport Media - 50, Nasal Swab - 50, Package Insert - 1, IVD, CE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Krishe Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
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.