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 May 19, 2021
Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator. Catalogue Number: CAL2351
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported May 19, 2021
ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St. Jude Medical, Cardian Rhythm Management Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 12, 2021
Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natrol, LLC
FDA (openFDA food enforcement)
Reported May 5, 2021
Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 5, 2021
Colpassist Vaginal Positioning Device - Product Usage: intended for use in general gynecological surgery to assist in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
Power Wheelchair
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merits Holdings Co. dba Merits Health Products, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
Philips Xper Flex Cardio (FC2010, Procedure Room and FC2020, Bedside Monitor) devices - intended for use by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Yellowfin Tuna portions Frozen IVP-CO Treated, Net WT 20 LBS, Size 1 LB.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quirch Foods
FDA (openFDA food enforcement)
Reported Apr 28, 2021
Dawn Food Products, 7 2 Layer Vanilla Bean Waterfall Cake, 35 oz., cake is placed on a cardboard plate which is then…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rise Baking Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 28, 2021
LogiCal Monitoring Set, Model Number DPS564898. for blood pressure monitoring and blood sampling.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then…
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 Apr 21, 2021
Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Cefprozil for Oral Suspension USP, 250mg/5mL, packaged as a) 50 mL (when mixed) bottles (NDC 68180-402-01); b) 75 mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Apr 21, 2021
Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Lite'n Foamy Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%), Net Contents: 18 oz/ 532 ml per foam pump…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spartan Chemical Co. Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 14, 2021
MicroScan WalkAway-40 plus Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Enteral Infusion Pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Medical Systems U.S.A., Inc.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
A610 Clinician Programmer Application for Deep Brain Stimulation Clinician Programming Guide Percept PC Model B35200…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Crimson Snapper Fillet, Natural Cut CO Treated, Net WT 10 LBS, Size 10/12 oz
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sea World, LLC
FDA (openFDA food enforcement)
Reported Apr 7, 2021
Alcon Custom Ophthalmic Surgical Procedure Packs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Apr 7, 2021
Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR, Evera S DR, Evera MRI XT DR, Evera MRI S…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 7, 2021
Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console, Model Numbers: 560BC, 560BC1, 560BCS, 560BCS1,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Apr 7, 2021
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions 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.