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 48,122 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Oct 9, 2013
McKesson Horizon Medical Imaging (HMI) Radiological Image Processing System, product versions 4.6.1 to 11.6., is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Information Solutions LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2013
BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Monaco RTP System Radiation treatment planning
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Bevacizumab 1.25 mg/0.05 mL PF, Avella Specialty Pharmacy, Phoenix, AZ, 85085, 877-782-7684
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avella
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 25, 2013
Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Sep 25, 2013
Coffee Cake: queso/guava (cheese/guava)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jean's Cake
3 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 25, 2013
"***SUPERPAN***Tu Pan Natural***"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lucy's Kitchen, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 25, 2013
BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture; Part Number: 72200775 Biodegradable suture anchor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc. Endoscopy Division
25 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products are contained within the Aequalis reversed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
*** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
Tec 6 continuous Flow Vaporizer and Tec 6 Plus Anesthesia Vaporizer. The Datex-Ohmeda Tec 6 Plus and Tec 6 Plus NAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Sep 18, 2013
ADVIA Centaur Folate (100 Tests), SMN 10310308, Cat No. 06367974 In vitro diagnostic use in the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2013
Dexpanthenol 250mg/ml PF, Qty: 1mL, WELLNESS PHARMACY, 1-800-227-2627
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wellness Pharmacy, Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 11, 2013
DMLC IV-ERGO - Beam shaping block for Radiation Therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2013
ADVIA Chemistry A1c_3 Calibrators, Catalog Number 10491408, IVD --- COMMON/USUAL NAME: ADVIA Chemistry A1c_3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics
FDA (openFDA device enforcement)
Reported Sep 4, 2013
buPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, 30-count tablets per bottle, Rx only, Distributed by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis South Atlantic LLC
FDA (openFDA drug enforcement)
Reported Sep 4, 2013
PrepStain AG. For use in the screening and detection of cervical cancer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Tres Leches cake sold under the following brand names: 1) "****Tres Leches***Postres D'Aqui***D'Aqui Manufacturing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.D'Aqui Manufacturing Products, Corp., dba Postres de Aqui
FDA (openFDA food enforcement)
Reported Sep 4, 2013
GE Ultrasound ViewPoint 6. Product Usage: ViewPoint is intended to be used in medical practices and in clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Integra Leyla Ball Joint Clamp, also as included in Leyla Table Mounting Hardware. The Leyla Retraction System, as part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra Limited
FDA (openFDA device enforcement)
Reported Sep 4, 2013
"***Que sos VACA NEGRA***CAP AEZ***Libre DE Lactose y Hormona R-BST***Quesos Vaca Negra, Carr 492 km 0.1, Hatillo,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Quesos Vaca Negra, Inc.
FDA (openFDA food enforcement)
Reported Sep 4, 2013
Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California Inc.
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.