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 Nov 25, 2020
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thomas Scientific
FDA (openFDA device enforcement)
Reported Nov 18, 2020
AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Mesalamine Delayed-Release Tablets, USP 1.2 gram, 120 tablets per bottle, Rx Only, Manufactured by: Actavis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Nov 4, 2020
Catapres (clonidine hydrochloride, USP) 0.1 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boehringer Ingelheim Pharmaceuticals, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 4, 2020
Equinoxe Platform Fracture Stem, 6.5mm, Left - Product Usage: The Equinoxe Platform Fracture Stem is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Invivo Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Rashkind Balloon Septostomy Catheter, 6F, Recess Balloon, Closed end, 50 cm, Pediatric, Single Lumen Product number:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Langston Dual Lumen Catheter
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2020
DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instrument Tray for EMPOWR Porous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Oct 14, 2020
NYSTATIN ORAL SUSPENSION, USP 100,000 units per mL Contains: Alcohol 0.5% v/v (Bubblegum Flavored) 16 fl. oz. (480 mL)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported Oct 7, 2020
Pacific Xtreme (PTCA Balloon Dilation Catheter)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ev3 Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Buprenorphine Transdermal System 5 mcg/hour, 4 transdermal systems/4 disposal units per carton, Rx Only, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Sep 30, 2020
Speed Stitch Needle Cassette
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol, REF 33570.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Potassium Acetate Injection, USP 40 mEq/20 mL (2 mEq/mL) Single Dose Vials, Rx only, Manufactured By: Exela Pharma…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Exela Pharma Sciences LLC
FDA (openFDA drug enforcement)
Reported Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novarad Corporation
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Lactate Dehydrogenase L-P, (LDH) (NAO), Catalog Number LD3842 - Product Usage: device intended for the quantitative in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, 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.