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 Aug 19, 2015
PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of…
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 Aug 19, 2015
Trumpf Ceiling Mounted Surgical Lighting Systems,iLED 3/5, User Manual #1558932. The TRUMPF surgical lights are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2015
Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort…
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 Aug 12, 2015
Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2015
Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC 0135-0135-02), b) 60 count…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.GlaxoSmithkline Consmer Healthcare
FDA (openFDA drug enforcement)
Reported Aug 12, 2015
Mometasone Furoate Ointment USP, 0.1%, 15 g tubes, Rx Only, Manufactured by Perrigo, Yeruham 80500, Israel, Distributed…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Perrigo Israel Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Aug 12, 2015
Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart XL+ is intended for use in a hospital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Aug 12, 2015
S2 Fluid Pack on the Cobas b 221 system- Catalog Number 03260925184 Blood Gas and Electrolytes Analyzer; The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2015
Nisoldipine Extended Release Tablets, 17 mg, packaged as a) Sular (nisoldipine) Extended Release tablets, 100-count…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Shionogi Inc.
FDA (openFDA drug enforcement)
Reported Aug 5, 2015
COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray, 20 mcg/100 mcg per actuation*, 4 Grams, 120…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boehringer Ingelheim Roxane Inc.
FDA (openFDA drug enforcement)
Reported Aug 5, 2015
Fat Free Pasteurized Prepared Cheese Product: SOUTHHOME 12/12OZ AMERICAN FAT FREE YELLOW, 0788001319. ROUNDYS 12/12OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dairy Farmers OF America Inc.
33 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 5, 2015
Paragon Laboratory Management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Technologies, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
ACUSON S 1000, ACUSON S 2000, or ACUSON S 3000 ultrasound systems with software version C3, C3, C3, or C1. Model…
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 Aug 5, 2015
InjectionPlasty 1.0 Bone Void Filler; an injectable and biocompatible calcium phosphate bone void filler. Sterilized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Kinetics, LLC
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Mermaid Medical M-Biopsy Coaxial Introducer Needle, Coaxial Needle for M-Biopsy 18Gx10cm-PRO-MAG, RX Only. Single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mermaid Medical A/S
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001, 459800220161, 459800232931,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Intermezzo (zolpidem tartrate), sublingual tablet 3.5 mg, 1 tablet per pouch, 30 pouches per carton, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Purdue Pharma LP
FDA (openFDA drug enforcement)
Reported Jul 29, 2015
ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Amlodipine Besylate Tablets, 2.5 mg Tablets, Packaged in 90 Count Bottles, Rx Only. Manufactured by: Wockhardt Limited,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wockhardt USA Inc.
34 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 22, 2015
Rifampin for Injection, USP 600mg/vial in a 20mL vial, Rx only, Manufactured for Fresenius Kabi LLC 3 Corporate Drive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
FDA (openFDA drug enforcement)
Reported Jul 22, 2015
Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2), For Transdermal Use Only, 30 Systems (patches) per box, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kremers Urban Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug 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.