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 48,100 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Nov 23, 2016
Bupropion Hydrochloride Extended-Release Tablets, USP (XL), 300 mg, a) 90-count bottle (NDC 68001-264-05), b) 500-count…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amerisource Health Services
FDA (openFDA drug enforcement)
Reported Nov 23, 2016
Atrium Medical 8 Fr Trocar catheter, Sterile Model Number: 8408 Intended to facilitate the evacuation of air and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Pipeline Embolization Device (Pipeline Classic) The device is indicated for the endovascular treatment of adults (22…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics Inc., dba Ev3 Neurovascular
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Laboratories, FL, Inc.
FDA (openFDA drug enforcement)
Reported Nov 9, 2016
Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc., Lake Forest, IL 60045, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn Inc.
FDA (openFDA drug enforcement)
Reported Nov 9, 2016
Model 055: Thermophore Classic, Professional Quality, Deep-Heat Therapy, Model 055 Large 14' x 27", Model 056:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Battle Creek Equipment Co.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Gildess 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP), 21 count, (a) 3 blisters…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Par Pharmaceutical, Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 9, 2016
TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71322040, 71322041, 71322042, 71322043, 71322044, 71322045,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Desoximetasone Cream USP, 0.25% 100 g, Rx only, mfd. by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taro Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 2, 2016
da Vinci¿ Xi" Surgical System, model number IS4000, A70_P5x with P5 Software; General and Plastic Surgery: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
Invokamet (canagliflozin and metformin HCl) tablets, 150 mg/1,000 mg, 60-count bottle, Rx only, Finished product…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Janssen Ortho LLC
FDA (openFDA drug enforcement)
Reported Oct 26, 2016
VITROS Chemistry Products GLU Slides, REF/Product Code 170 7801 (300 slides per sales unit), Unique Device Identifier…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tearscience, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
PARICALCITOL Capsules, 1 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 26, 2016
Vascular Solutions Twin-Pass Dual Access Catheter, models 5200, 5210, and 5230. Sterilized with Ethylene Oxide. The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Calix P PEEK Lumbar System, PLIF Rasp
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Marcaine 0.25% (bupivacaine HCl) injection, USP, 125 mg/50 mL (2.5 mg/mL), 50 mL Multiple-Dose Vial, Rx only, Hospira,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc., A Pfizer Company
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 19, 2016
Symbia S, Product Usage 1) SPECT: To Detect or image the distribution of radionuclides in the body or organ, using 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)
Reported Oct 19, 2016
Amikacin Sulfate Injection, USP, 500 mg/2 mL (250 mg/mL) Rx Only, Manufactured in Hungary For: Teva Pharmaceuticals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 19, 2016
TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-Chair. Intended use is to provide the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2016
Michigan Turkey Producers Retira del Mercado Productos de Pavo Debido a una Posible Contaminacin Con Material Extrao
High riskUsing this product could cause serious injury, illness or death — stop using it now.Michigan Turkey Producers Co-op, Inc.
USDA FSIS
Reported Oct 12, 2016
Product in cans of 4 1/4 oz (111g) and 8 1/4 oz (220g) net weight. Label reading in part as: "Coloso***PULPO EN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ballester Hermanos, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 12, 2016
Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Panoramic Rental Corp.
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.