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.

6,421 stored notices name Florida, reported between Jun 20, 2012 and Sep 23, 2026.

Medical devices

Reported Sep 5, 2018

Stryker Mako Vizadisc Knee Procedure Tracking Kit

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

Mako Surgical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 5, 2018

MORTON NATURAL SEA SALT ALL PURPOSE***NET WET 26 OZ (1 LB 10 OZ) 737 g***Nutrition Facts***INGREDIENTS: SEA SALT…

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

Morton Salt Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 5, 2018

QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap…

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

Stryker Leibinger GmbH & Co. KG

17 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 30, 2018

Publix Super Markets Inc. Recalls Ground Chuck Products Due To Possible E. coli O26 Contamination

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

Publix Supermarkets, Inc., Deli Plant

USDA FSIS

Medical devices

Reported Aug 29, 2018

BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…

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

CAREstream Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an…

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

Compass Health Brands (Corporate Office)

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

BEST TASTE BRAND SNACK GINGER SLICED, Net Weight 200g, 7 OZ, Distributed by; COUNTRY FAVOR., INC U.S.A; PRODUCT OF…

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

Country Favor Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…

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

GE Healthcare Japan Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN…

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

Graeters Manufacturing Company

FDA (openFDA food enforcement)

Food

Reported Aug 29, 2018

Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend, Net Wt. 15 lbs (6 / 2.5 lb bags per case), UPC…

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

J R Simplot Co. Corporate HQ

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…

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

Liebel-Flarsheim Company LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000

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

O-Two Medical Technologies, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…

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

Salt & Straw LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

3D TOP Ceiling Stand, model no. 3070039 3074486 3070013 3070021 Product Usage: The ceiling stand is used to hold the…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag, and 4 oz., and 2…

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

Teasource

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

The Tri-Flo Subglottic Suction System

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

Vyaire Medical

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Connecting Bolt, Model 14-442093

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)

Medical devices

Reported Aug 22, 2018

Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with…

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

Apollo Endosurgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath…

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

Arrow International Inc.

1 more product 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.