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.
6,511 stored notices name Florida, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Florida too — those are in the archive.
Reported Oct 21, 2026Updated Oct 26, 2026
Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Nov 2, 2026
Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Made From Plants; Daring; Plant Steak Bites; Ready in 4 Mins Microwaveable Pouch; UPC: 86001124319
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daring Foods Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product Code: N271H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Instrumentation Laboratory
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jenavalve Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 4099100167023
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
J. HIGGS Loaded Bacon & Cheddar Potato Chips, NET WT 7.75 OZ (219.7g) bag, UPC 051933316454. Sold as 13 (7.75oz) bags…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Saratoga Potato Chips LLC
FDA (openFDA food enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SI-BONE, Inc.
FDA (openFDA device enforcement)
FoodReported Oct 16, 2026Updated Nov 3, 2026
Lidl US Recalls Gelatelli Coffee & Vanilla Gelato Due to Possible Health Risk
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Lidl US
FDA (recalls & safety alerts)
Reported Oct 14, 2026Updated Oct 20, 2026
DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVID Medical, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2026
Erytra Automated Blood Grouping and Antibody Test System, Templates Pack versions 15.0.0 and 16.0.0, Model no. 210400,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Grifols, S.A.
FDA (weekly enforcement report)
Reported Oct 14, 2026Updated Oct 20, 2026
Cranberry Chicken Salad Wedge 4.5 oz package in Wedge plastic and clear container with a plastic film sealing the top.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Freshpoint Central Florida, Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
LEASA Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 6 OZ. (170g); Grown &…
High riskUsing this product could cause serious injury, illness or death — stop using it now.LEASA Industries Co., Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026
LEASA Living Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 4 OZ. (113g); Grown…
High riskUsing this product could cause serious injury, illness or death — stop using it now.LEASA Industries Co., Inc.
FDA (weekly enforcement report)
Reported Oct 14, 2026Updated Oct 20, 2026
TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, 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.