Recalls distributed in Puerto Rico
These notices name Puerto Rico 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.
2,528 stored notices name Puerto Rico, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Jul 22, 2015
Sorin Stockert Heater-Cooler 3T, 230 V Temperature control for extracorporeal perfusion of durations up to 6 hours.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
G7 Variant Elution Buffer HiS no. 1 (M) component of the Tosoh Automated Glycohemoglobin Analyzer HLC 723G7. Product…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alliance Partners LLC
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Losartan potassium tablets USP, 25 mg, 90- count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 15, 2015
0.9% Sodium Chloride Injection, USP, in 250mL VIAFLEX Plastic bags, Manufactured by Baxter Healthcare Corporation 65…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corp.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 15, 2015
Siemens Healthcare Diagnostics Dimension Vista Systems, used with the Dimension Vista Intelligent Lab System software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
ICT Serum Calibrator REF 146-03. For use in the calibration of the serum Sodium, Potassium, and Chloride assays.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jul 8, 2015
GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A universal diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
INSTRUMENT ARM DRAPE, IS4000, 20 PACK; used on the da Vinci Xi Surgical System. The Intuitive Surgical Endoscope…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue. Model Number STA-5050-305. The Wand…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Milestone Scientific, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use on the Hitachi systems for The quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal lubricant.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sheffield Pharmaceuticals, LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2015
The Rapidlab 1260 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP), 28 day Regimen, 6 Tablet Dispensers per box,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Inc.
FDA (openFDA drug enforcement)
Reported Jul 1, 2015
BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blue Bell Creameries, LP
285 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
GE Healthcare, Treadmill T2100. For Exercise Testing, facilitating accurate blood pressure measurements and exercise…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Dr Blue Pain Relieving Gel, (4.6% menthol), For temporary relief of minor aches and pains of muscles and joints, a) 2…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Indiana Botanic Gardens, Inc.
FDA (openFDA drug enforcement)
Reported Jul 1, 2015
VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2015
ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended for Meniscal Repair.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Fios First Entry; 5mm x 100mm and 12mm x 100mm; Model #:CTF03 and CTF73. Indicated for use to establish a port of entry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 24, 2015
Neusoft NeuViz 64 Multi-slice CT Scanner System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neusoft Medical System Co.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088; Part Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, 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.