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 Aug 9, 2023
NeuMoDx Cartridge-used for extraction, purification, amplification and detection of nucleic acids on the NeuMoDx 288…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuMoDx Molecular Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
Ringed DxI Reaction Vessels (RVs)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
SPRING VALLEY brand POTATO BLINTZES; NET WT. 13 OZ (369g); KEEP FROZEN; READY TO COOK; INGREDIENTS: WHEAT FLOUR (WHET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Milmar Food Corp.
FDA (openFDA food enforcement)
Reported Aug 2, 2023
QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and differentiation of nucleic acid from…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
vRad PACS with Mammography
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Virtual Radiologic Corp.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
Trader Joes Unexpected Broccoli Cheddar Soup ( Sharp Cheddar Cheese & Unexpected Cheddar Cheese )Keep Refrigerated, NET…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Winter Gardens Quality Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 26, 2023
Contour¿ next GEN Blood Glucose Monitoring System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascensia Diabetes Care US, Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Soft Cream Spread, Net Wt 16oz (1lb)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Central America Products Corporation
FDA (openFDA food enforcement)
Reported Jul 26, 2023
RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cytocell Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Trader Joe s Organic Tropical Fruit Blend Pineapple, Banana, Strawberry, Mango, SKU #051191, packaged in pillow bags.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Scenic Fruit Company, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 19, 2023
HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Medtronic Catalyft LS Expandable Interbody System, Anterier Standalone Cage, REF 981023322, spinal implant
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2023
REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amin Trading Agency LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NeuMoDx Molecular Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
A20180 BATTER MIX X4 50.00 BAG
High riskUsing this product could cause serious injury, illness or death — stop using it now.Newly Weds Foods, Inc.
195 more products in this recall
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.