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 Jul 12, 2023
Pearl Milling Company Self-Rising Yellow Corn Meal Mix Net Wt 80 oz (5 lb) UPC 3000057380 packaged in paper bag with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PepsiCo Beverages & Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pro-Dex Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quidel Cardiovascular Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Aptio Automation Storage and Retrieval Module (SRM)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2023
1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an amber glass bottle; 2. Sonne's Calphonite #2, 15 Fl. oz. (444…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Anatox Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 5, 2023
Voalte Patient Safety, Part Number 4.0, V4.0.000 to 4.0.401, used with the Centrella Bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Access Hybritech p2PSA reagent, REF B03704 and REF A49752.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DRE Medical Group Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Exactech Shoulder GPS Impactor Handle, Catalog #531-07-05.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2023
LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-82NE; LEGACY SMARTBASE NARROW…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). Individual units are packaged in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Motts LLP
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ingredients: Fish Protein (Pollock, Threadfin Bream and/or…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aquamar Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
enterade Advanced Oncology Formula; Original Vanilla Flavor; Medical Food; Helps manage and maintain GI function; 8 FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Entrinsic Health Solution Inc.
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Serrated Blade Applicator Kit (12 Sample), REF: 552687, For use with the Spife Nexus system, Contents: 30 Blade…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
Julian's Recipe Original Cauli-Wafels, 7.41 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Julian's Recipe, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2023
KARL STORZ Radel Sterilization Trays, Models: 27717A, 27717B, 39301A, 39301C, 39231XA, 39301C1, 39311A, 39317A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2023
Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor, REF: 4053
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 Jun 28, 2023
TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g) UPC: 749735002186 Product is a powder packed metal cans. 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
FDA (openFDA food enforcement)
Reported Jun 28, 2023
V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SenTec AG
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Eye and Ear Dropper, Product Code 67082
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apothecary Products, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992206 Version A, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
12 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.