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 Jul 10, 2019
Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging sources, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
CLEO Patient Monitor /Tranquility VS Patient Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Infinium Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent, Product Number HY0305Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food enforcement)
Reported Jul 10, 2019
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2019
Parivar brand Dry Dates (Kharek) Net Wt.14 oz. (400 g) Product of India Batch No. 127/BHBI
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dilip Ceramics dba Shivam Distribut
FDA (openFDA food enforcement)
Reported Jun 26, 2019
Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm, 5FR/50cm, Catalog Number ASB5-35-50-6-4, REF Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2019
Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cytocell Ltd.
FDA (openFDA device enforcement)
Reported Jun 26, 2019
2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2019
CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04 - Product Usage: The Tilting Head…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med Tec Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2019
Robafen DM, Generic for Robitussin DM, In each teaspoonful (5mL): Dextromethorphan HBr, USP 10mg,/Guaifenesin, USP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Sandwich. Horchata Rice Milk & Cinnamon frozen dessert…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Coolhaus
FDA (openFDA food enforcement)
Reported Jun 19, 2019
IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jun 19, 2019
Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 19, 2019
xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Molecular Diagnostics
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Jun 12, 2019
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.I.T.S. GmbH
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerr/Pentron, dba Kerr Corporation and Pentron Clinical
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NxStage Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F
High riskUsing this product could cause serious injury, illness or death — stop using it now.OriGen Biomedical, Inc.
5 more products in this recall
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.