All recall categories

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.

Food

Reported Sep 2, 2026Updated Sep 16, 2026

hodo CHILI CRISP LIGHTLY FRIED TOFU. NET WT 8oz. KEEP REFRIGERATED. Manufactured by: Hodo Inc., Oakland, CA 94608. UPC:…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Hodo Inc.

FDA (weekly enforcement report)

Drugs

Reported Sep 2, 2026Updated Sep 16, 2026

IV Sets with drip chambers

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 2, 2026Updated Sep 7, 2026

Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2026Updated Sep 7, 2026

POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting &…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Sep 2, 2026Updated Sep 16, 2026

Double Golden Fish Galanga Powder, 2.3 .oz, plastic jar, 48 per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tang's Family Corporation

FDA (weekly enforcement report)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrowhead DE LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

BMC/REACTHEALTH Luna G3 APAP REF LG 3600

High riskUsing this product could cause serious injury, illness or death — stop using it now.

BMC Medical Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intersurgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kico Knee Innovation Company

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalized poly pillow…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nutrient Foods, LLC

FDA (openFDA food enforcement)

Drugs

Reported Aug 26, 2026Updated Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OneBlood, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Paragonix Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 26, 2026Updated Sep 13, 2026

Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Publix Super Markets, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SDI Limited

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF(s):L2kSY2/10489085; L2KSY6/10488319 IVD, RxOnly

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Products Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 26, 2026Updated Sep 16, 2026

Whole Blood

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Suncoast Communities Blood Bank, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Food

Reported Aug 19, 2026Updated Sep 7, 2026

Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

529 Commerce, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Sep 7, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Erbe USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microvention 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.