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 Dec 11, 2019
Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frog Hollow Farm
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Proximal Humerus Plate, 8 holes, Right, REF MDS130108R - Product Usage: The Proximal Humerus Plating System consists of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Miami Device Solutions, LLC.
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Sullivan Harbor Farm Smokehouse Refrigerated, Ready-to-Eat, Cold Smoked Salmon in vacuum packaging (4 oz., 8 oz., 1…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mill Stream Corp.
FDA (openFDA food enforcement)
Reported Dec 11, 2019
TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Theralase Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
PANTERA Proximal Humerus Fracture Plate System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toby Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Pasteurized Process American Cheese, white, 6 - 5lb loaves per case. Brands as follows: 1) Foodtown; 2) Hannaford; 3)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Great Lakes Cheese Co. Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 4, 2019
North Bay Produce brand McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples sold in 2 lbs and 3 lbs…
High riskUsing this product could cause serious injury, illness or death — stop using it now.North Bay Produce Inc.
FDA (openFDA food enforcement)
Reported Dec 4, 2019
Ibuprofen Oral Suspension USP, 100 mg/5mL, 4 fl.oz. 118 mL, Rx only, Preferred Pharmaceuticals, Inc., Anaheim, CA. Mfg:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2019
Atellica CH 930 Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMD Medicom Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Parivar brand Dry Dates (Kharek) Net Wt.7 oz. (200 g) and 14 oz. (400 g) Product of India Batch No. 125/BIBT
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 Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hager & Meisinger GmbH
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Dry dates packaged under the following brands: Keshav Dry Yellow Dates, 7oz., UPC: 643864233124 and 14oz., UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peekay International, Inc.
FDA (openFDA food enforcement)
Reported Nov 27, 2019
TEMPLE PURE PRANA MATCHA+SHOT; 3 FL OZ (89mL); VITALITY SUPERBOOST; COLD PRESSURED; PERISHABLE KEEP REFRIGERATED;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Temple Turmeric Inc.
FDA (openFDA food enforcement)
Reported Nov 22, 2019
Ajinomoto Foods North America, Inc. Retira Productos De Arroz Frito Con Pollo Debido A Una Posible Contaminación Con…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ajinomoto Foods North America
USDA FSIS
Reported Nov 21, 2019
Missa Bay, LLC Recalls Salad Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay LLC
USDA FSIS
Reported Nov 20, 2019
Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadence Science, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) - Product Usage: The catheterization table is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galil Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
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.