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 Jul 6, 2016
Ciprofloxacin Ophthalmic Solution (0.3% as base), Sterile, Rx only, a) 2.5 mL Bottle, b) 5 mL Bottle, c) 10 mL Bottle,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Pharma Inc.
FDA (openFDA drug enforcement)
Reported Jul 6, 2016
Access Free T3 Assay, Ref No. A13422 The Access Free T3 assay is a paramagnetic particle, chemiluminescent immunoassay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
MOSAIQ Oncology Information System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Lisinopril & Hydrochlorothiazide Tables, USP 20mg/12.5mg, packaged in a)100-count bottles and b) 5000-count bottles, Rx…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jul 6, 2016
Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nephron Pharmaceuticals Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Bronchoscope Intended to provide optical visualization of and therapeutic access to the Airway and Bronchial Tree. This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax Medical Company
15 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2016
LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External Defibrillator(s) and are non-wearable. LIFEPAK CR Plus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 3 LEFT, A/P 54.5 MM, M/L 62 MM, REF 71421373 The LEGION Hinge Knee System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 29, 2016
Let's Talk Health Energizer Drink Mix Citrus 0.3oz UPC #91131180631
High riskUsing this product could cause serious injury, illness or death — stop using it now.Let's Talk Health, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 29, 2016
Hyoscyamine Sulfate Sublingual Tablets, 0.125 mg, packaged in 100-count bottles, Rx only, Manufactured for: Virtus…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Virtus Pharmaceuticals, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 22, 2016
Label reads in part as: "Clight***Naranja*** Orange***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Puerto Rico
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 22, 2016
Natus neoBLUE Phototherapy system, Catalogue Part Number: 010066. Top Assembly Part Numbers: 001103, 001314, 002110,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jun 22, 2016
Oasis Foods Canola Fry Shortening, Net Wt. 35 LB (15.88), Distributed by: Oasis Foods, Inc. Hillside, NJ 07205, UPC 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oasis Trading Co., Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 22, 2016
Pramipexole Dihydrochloride Extended Release Tablets, 0.375 mg, Rx Only, 30 count bottles, Manufactured By: Par…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Par Pharmaceutical
FDA (openFDA drug enforcement)
Reported Jun 22, 2016
LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature installed. Part numbers: V15-2-xxxxxx (includes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Jun 22, 2016
The XN-Series modules (XN-10, XN-20) are quantitative multi-parameter automated hematology analyzers intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex Corporation
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Actifuse ABX/Actifuse MIS System A bone void filler intended only for orthopedic applications as a filler for gaps and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apatech Limited
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Lipase, Catalog No. OSR6x30 Product Usage: Lipase OSR6x30 is intended as a System reagent for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
VITROS 3600 Immunodiagnostic System, Catalog Number 6802783,for use in the in vitro quantitative, semi-quantitative,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Sulfacetamide Sodium Ophthalmic Solution, USP, 10%, Sterile, Rx Only, 15 mL bottles, Mfd. by: Akorn, Inc., Lake Forest,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
FDA (openFDA drug enforcement)
Reported Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
COSEAL Surgical Sealant Kit, 2 mL, Product Code: 934070; For use in vascular reconstructions to achieve adjunctive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
SEAL,IS4000 PORTS,5MM-8MM,BOX of 10; Model numbers: 470361-03, 470361-04, 470361-05, 470361-06; Part number: 470361.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, 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.