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 15, 2025
VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maquet Cardiovascular, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2025
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Unitek Corporation
FDA (openFDA device enforcement)
Reported Jan 8, 2025
--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grimmway Enterprises, Inc. dba Grimmway Farms
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2025
The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jan 1, 2025
20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD FACSLyric" flow cytometer is intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Bio Sciences
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
Monitoring Service Application (MSA). Software to process, analyze, display, and report cardiac events in ECG data…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Braemar Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Jan 1, 2025
StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685. Prescription use blood glucose meter for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nova Biomedical Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straight Smile, LLC
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil, straight. Model/Catalog Number: 14-5011 The Disposable…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kirwan Surgical Products, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER NO Y-SITE 25120 EDMS II 25120 BECKER W/1-WAY…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Neurosurgery
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Dec 18, 2024
BD Pyxis MedStation ES, REF: 323
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2024
MICRO-X Rover Mobile X-ray System, # MXU-RV35
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-X Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2024
Levothyroxine Sodium Tablets USP, 125 mcg, packaged in a) 90-count bottles (NDC 0378-1813-77) and b) 1000-count bottles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viatris Inc.
10 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 11, 2024
Duloxetine Delayed-Release Capsules, USP, 20 mg, Rx only, 60 count bottles, Manufactured by: Aurobindo Pharma Limited,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerisource Health Services LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 11, 2024
BD EpiCenter Single User Software Version or Model: 441007 Catalog Number: 441007
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2024
Ziehm Solo. Digital Mobile C-arm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthoscan, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2024
AMS Artificial Urinary Sphincter Control Pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2024
MICRO-X Rover Mobile X-ray System, # MXU-RV35
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-X Ltd.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-1.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caire, Inc.
3 more products 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.