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 Jan 4, 2017
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
AbbVie PEG Kit 20 FR
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AbbVie Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
AMGEN Kyprolis (carfilzomib) for injection, 30 mg per vial, Discard unused portion, For Intravenous Administration…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amgen, Inc.
FDA (openFDA drug enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 slides per sales unit), Catalog # 1926740 and 2) ,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Dec 28, 2016
OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Is designed to facilitate the introduction of catheters…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oscor, Inc.
29 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
COMFORT SHIELD (dimethicone) Barrier Cream Cloths, 3%, packaged as impregnated cloths wrapped in flexible packaging,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sage Products LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 28, 2016
Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultroid Technologies, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Virtus Pharmaceuticals Opco Ii L
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 21, 2016
GE Healthcare, Avance, Avance CS2, Amingo.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GF Health Products, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jubilant Cadista Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Dec 21, 2016
Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides phototherapy underneath the infant and can be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 count box, Rx Only, For Spinal Anesthesia…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Dec 14, 2016
Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a software application that is used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mondelez International
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
ADVIA 560 Hematology Systems, Siemens Material Number (SMN) 11170842, IVD.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library, V6 Spectrum Infusion Pump, Product Code 35700BAX and…
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 Dec 7, 2016
Salsalate Tablets, USP, 500 mg, packaged in a) 500 count bottles (NDC 42937-703-18); b) 100 count bottles (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nationwide Laboratories, LLC
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 7, 2016
MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
ST¿CKERT HeaterCooler System 3T; Item Number 160281, HeaterCooler 3T, 240V/60Hz; Item Number 160282,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Turbo Elite Atherectomy Catheter. Models: 410-152, 410-154, 414-151, 414-159, 417-152, 417-156, 420-006, 420-159,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
2 more products in this recall
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.