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 29, 2020
iChem VELOCITY Urine Chemistry Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2020
VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Fast-Cath Trio HEMOSTASIS INTRODUCER, 14F, 4.6 mm, REF 406303
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2020
MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
FDA (openFDA drug enforcement)
Reported Jan 8, 2020
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nidek, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent System. The SMART stent system includes a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alliance Tech Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2019
A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Chef Pineiro's Sofrito con Cilantro, with Coriander, NET WT./PESO NETO 12 oz (340g) and NET WT./PESO NETO 32 oz (907g)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AC Culinary Group LLC.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 18, 2019
EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Ligamax 5 mm Endoscopic Multiple Clip Applier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Dec 11, 2019
Onion Minced: 16-40 Mesh, Net Weight: 24/kg/52.91lbs, Manufacturing Date: May, 2019, Country of Origin: China,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gh Imports, Inc.
FDA (openFDA food enforcement)
Reported Dec 11, 2019
PANTERA Proximal Humerus Fracture Plate System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toby Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Atellica CH 930 Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Basic Reset Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 27, 2019
Randox Liquid Cardiac Controls Catalogue Number CQ5051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
WECK AutoEndo5, Automatic Hem-O-Lok Clip Applier, REF AE05ML Automatic Endoscopic Surgical Ligating Clip Appliers are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
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.