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 48,123 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Jul 31, 2013
GE Healthcare Infinia Hawkeye 4 Option For Dual-Head Variable Angle Gamma Camera, Hawkeye Option for Dual-Head Variable…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
ARTIS zee and zeego x-ray, angiographic system with Software Artis VC20x/VC21A that have Patch 7 and a 3D and DSA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Eon and Eon Mini charging system, model numbers Eon -3701 (Wall Charger), 3711 (Portable Charger) and Eon Mini -3721…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical
FDA (openFDA device enforcement)
Reported Jul 24, 2013
ExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple sterile ingredients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxa Corporation
FDA (openFDA device enforcement)
Reported Jul 24, 2013
Oxytocin Injection, USP, (Synthetic), 10 USP Units/mL, for IV Infusion or IM Use, Rx Only, 1 mL vial, APP ) 10 USP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
FDA (openFDA drug enforcement)
Reported Jul 24, 2013
Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus Product Usage: Angiographic x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2013
Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Usage: Eon: Eon system is indicated as an aid in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2013
CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
Baxter's elastomeric infusion pumps are non-electronic, ambulatory, disposable devices that deliver continuous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
RigiflexTM 11 Single-Use Achalasia Balloon Dilator, Material Number (UPN) M00554510 Product Usage: The Boston…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
Benztropine Mesylate Injection, USP, 2 mg/2 mL (1 mg/1 mL), 2 mL Single Dose Vial, Rx only, labeled as a) Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 17, 2013
Acetyl-D-Glucosamine w/Chondroitin 200 mg/ml, compounded by Olympia Pharmacy, Orlando, FL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lowlite Investments, Inc. D/B/A Olympia Pharmacy
104 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 17, 2013
Nimodipine Capsules 30 mg, Rx Only, For Institutional Use Only, a) 30-count unit dose Capsules (5x6 blister cards per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sun Pharmaceutical Industries Inc.
FDA (openFDA drug enforcement)
Reported Jul 10, 2013
0.9% Sodium Chloride Injection, USP, in MINI-BAG Plus Container, a) 50 mL (NDC 0338-0553-11), b) 100 mL (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 10, 2013
HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clorox Healthcare Holdings, LLC (dba HealthLink)
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
1) VITROS 5,1 FS Chemistry System (product code 6801375) and 2) VITROS 5,1 FS Chemistry System Refurbished (product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625 mg/2.5 mg, 1 blister card containing 28…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 10, 2013
Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL), 0.01 %, 118.28 mL (4 Fl. oz.) bottle, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hill Dermaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jul 3, 2013
0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7983-30), b) 1000 mL (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
8 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 3, 2013
INFUSE(R) Bone Graft, SMALL KIT, REF 7510200, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2013
VITROS Chemistry Products K+ (Potassium) Slides (Reagent), REF/Catalog Number 815 7596, Product Usage: For in vitro…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2013
HydrOXYzine Hydrochloride Oral Solution, USP, 10 mg/5 mL, 16 fl. oz. (473 mL), Rx Only, HI-TECH PHARMACAL CO., INC.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., Inc.
FDA (openFDA drug enforcement)
Reported Jun 26, 2013
0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA drug 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.