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. A further 48,132 notices were distributed nationwide, so they reach Florida too — those are in the archive.

Medical devices

Reported Nov 6, 2019

Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…

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

OrthoPediatrics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…

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

Pajunk GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

POM Procedural Oxygen Masks, Endoscopic, Conscious Sedation, Bronchoscopy Mask, as follows: (1) POM Medical, LLC, REF…

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

POM Medical LLC

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…

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

Rong Shing Trading NY Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Dried Date NET WT: 12 oz(340g+/-5g) packed in clear plastic bag. Product of China. INGREDIENTS: DRTED DATE; Packed By:…

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

Super World Trading Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Posey Connected Twice-As-Tough Cuffs

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

Tidi Products

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Ample Hills Peppermint Pattie ice cream packed in 3 gallon tubs and half pint (8oz) cartons . Allergens: Contains:…

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

Ample Hills Manufacturing

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

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

Andover Healthcare Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm

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

CrossRoads Extremity Systems, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

IMRIS MR/X-ray head fixation device, Model HFD200

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

Deerfield Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

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

IrriMAX Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software…

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

Life Technologies Holdings Pte Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz., with UPC code 612510002032.

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

Lipari Foods Operating Company, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic…

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

Mrs. Stratton's Salads, Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 30, 2019

Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…

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

Roland Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD 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.