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.

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Presource Convenience Kits: 1) KIT, PRE OP , Catalog Number: AMN548616A; 2) KIT, NICU ADMIT NEW HAN , Catalog Number:…

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

Cardinal Health 200, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 15, 2026

INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model…

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

CooperSurgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

CorneaGen - Boston

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…

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

Criticare Technologies, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated

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

OneBlood, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12

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

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Bone

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

Tissue Transplant Technology, Ltd.

FDA (weekly enforcement report)

Food

Reported Sep 30, 2026Updated Oct 7, 2026

Reese's Crunchy Peanut Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice…

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

Unilever North America Supply Chain Company, LLC

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve

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

Ventec Life Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 25, 2026Updated Oct 30, 2026

Fontanini Foods LLC Recalls Raw, Frozen Pork Sausage Products Due to Possible Foreign Matter Contamination

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

Fontanini Foods, LLC

USDA FSIS

Meat & poultry

Reported Sep 25, 2026Updated Oct 25, 2026

Sempio Food Services Inc. Recalls Ready-To-Eat Chicken Stew Products Imported Without the Benefit of Import Reinspection

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

Sempio Food Services Inc.

USDA FSIS

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

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

Bard Access Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHOLE GRAIN OATS, MILK, MARGARINE***WATER, SALT, CONTAINS LESS…

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

Best Friends Bakery, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100

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

embecta Medical II LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

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

Happiest Baby, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Plum administration sets

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

ICU Medical, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software…

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

Nuclein LLC

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2…

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

Optimus Inc. d/b/a/ Markys Caviar

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Philips Patient Information Center iX REF:866389

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

Philips North America

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006

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

restor3d Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

GM Helix Implant, REF: 109.984;

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

Straumann USA LLC

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.