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 48,123 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Nov 7, 2012
Software for Vitrea, Vitrea fX, and Vitrea Enterprise Suite (VES): VPMC-09293C Vitrea . Model Number Vitrea 5.2, 6.0,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Images, Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxa Corporation
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Synchron Systems Synchron Calibrator Multi Calibrator Diskettes, Part Number 442600. The SYNCHRON MULTI-CALIBRATOR,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only BiCNU manufactured by: Ben Venue Laboratories, Inc.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bristol-myers Squibb Company
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 31, 2012
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospira, Inc., Lake…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Oct 31, 2012
Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP, 1 mg/35 mcg, inert tablets, 28-count tablets per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Watson Laboratories Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 24, 2012
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Belmont Instrument Corporation
FDA (openFDA device enforcement)
Reported Oct 24, 2012
"Sofrito a Mi Gusto***100% Natural (Natural Seasoning)***Keep Refrigerated***Elaborado y Envasado por Ernesto Tropical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ernesto Tropical Food, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 24, 2012
Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Oct 24, 2012
"Tacos de Langosta" (Lobster-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sun Boricua Pa'l Mundo Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 17, 2012
Prometh VC Plain, Each 5mL contains: Promethazine Hydrochloride 6.25mg & Phenylephrine Hydrochloride 5mg, One Pint…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Mid Atlantic LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 17, 2012
Triage TOX Drug Screen Panel, Model# 94400. Product Usage: The Triage TOX Drug Screen is a fluorescence immunoassay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2012
IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Animas Corporation
FDA (openFDA device enforcement)
Reported Oct 10, 2012
8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc balloon. The product is packaged individually with 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc., Urological Division
FDA (openFDA device enforcement)
Reported Oct 10, 2012
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx Only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A. NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mylan Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Oct 10, 2012
00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys Femoral Head Provisional 22mm +3.5 00789502220…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
FDA (openFDA device enforcement)
Reported Oct 3, 2012
5% Dextrose Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E0062, NDC 0338-6346-02; b) 500 mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 3, 2012
Trinity Biotech, Captia VZV IgG. Product code 2325600: 96 Tests; product code: 2325601: 480 tests. For in vitro…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clark Laboratories, Inc. (dba,Trinity Biotech USA)
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Imager
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haag-Streit USA Inc.
FDA (openFDA device enforcement)
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Other states
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.