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 Mar 5, 2014
PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error that does not…
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 Feb 26, 2014
Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2014
Trelstar (triptorelin pamoate) for Injectable Suspension Single-Dose Vial (NDC 52544-154-02) plus MIXJECT Single-Dose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Actavis Inc.
FDA (openFDA drug enforcement)
Reported Feb 19, 2014
VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only. Manufactured by E-Z-EM Canada Inc. a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bracco Diagnostics Inc.
FDA (openFDA drug enforcement)
Reported Feb 19, 2014
Horizon Medical Imaging, Picture Archive Communication System (PACS).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Information Solutions LLC
FDA (openFDA device enforcement)
Reported Feb 19, 2014
The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urinalysis. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex America, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
SmartSite Needleless Connector, Model No. 2000E The SmartSite Needleless Connectors are sterile, individually packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Pyridostigmine Bromide Tablets USP, 60 mg, 100 count bottle, Rx only, Manufactured and Distributed by: Corepharma, LLC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corepharma LLC
FDA (openFDA drug enforcement)
Reported Feb 12, 2014
XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only, Forest Pharmaceuticals Inc., St.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Forest Pharmaceuticals Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 12, 2014
Giraffe¿ Infant Warmers, part number M1118179, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Greenstone LLC
FDA (openFDA drug enforcement)
Reported Feb 12, 2014
Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe, Rx Only. Manufactured by: Insight Instruments, Inc., 2580 SE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Insight Instruments, Inc.
FDA (openFDA drug enforcement)
Reported Feb 12, 2014
MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nipro Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Ofloxacin Ophthalmic Solution, USP 0.3%, 5mL, (NDC 16571-130-50). The products are packaged in Low Density Polyethylene…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.PACK Pharmaceuticals, LLC
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 12, 2014
Glucotrol XL (glipizide) extended release tablets, 5 mg, 100 count bottles, Rx only, Distributed by Roerig, Division of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2014
BuPROPion Hydrochloride Extended-Release Tablet (XL) 150mg, Rx only, a) 30 count bottle(NDC 0591-3331-30), b) 90 count…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2014
Soliris (eculizumab) Concentrated Solution for Intravenous Infusion Only, 300 mg/30 mL (10 mg/mL), 30 mL Single-Use…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alexion Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2014
ZYM B Reagent (REF 70493) ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux France Chemin De L'Or
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2014
KETOCONAZOLE CREAM, 2%, 30 gram tube, Rx only, E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc., Melville,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Fougera Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2014
Aminosyn 3.5% M Sulfite-Free, A Crystalline Amino Acid Solution* with Maintenance Electrolytes with Phosphorus, 1000 mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 5, 2014
Hydravax High Potency Diuretic Weight Loss Solution, Pharmaceutical Grade, 45 capsules per bottle, Dietary Supplement,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.IQ Formulations, LLC
FDA (openFDA drug enforcement)
Reported Feb 5, 2014
Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw Driver, Product Usage: The Modular Screw Driver…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix, 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.