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 Sep 16, 2015
DermaPen Pro Model, Micro Needling System, a motorized AC powered surgical instrument for dermabrasive use. Each…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Derma Pen, LLC
FDA (openFDA device enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 9, 2015
COULTER LH Series Diluent, Catalog No. 8547194, Product Labeling A40192-AD. The diluent provides the ability to analyze…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2015
ANGIODRAPE PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Customed, Inc.
169 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2015
KimVent* Closed Suction System for Adults, 12 F, T-Piece (Product Code 2155); KimVent* Closed Suction System for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
31 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2015
VITROS 5,1 FS Chemistry System, Catalog Number/Product Code 6801375, Unique Device Identifier No. 10758750001132, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Panoramic X-ray Model PC-1000 The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser 1000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Panoramic Rental Corp.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Qualitest Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Sep 9, 2015
Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Sep 2, 2015
LX3 Floor Stand for Endure Luxite Envision Optical System; Endure LuxOR Q-Vue. Product Usage: The LX3 Microscope Floor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
MiniCap Extended Life PD Transfer Set Extra Short (4") with Twist Clamp. Product Code: 5C4483. intended for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Bactroban (mupirocin calcium) Nasal Ointment, 2% 1g tube, Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GlaxoSmithKline, LLC.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 2, 2015
iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049, 800-3050, 800-3079, 800-3080, 800-3530, 800-7167,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iris Diagnostics
FDA (openFDA device enforcement)
Reported Sep 2, 2015
cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a fully automated POC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bromfenac Ophthalmic Solution, 0.09%, 1.7 mL Bottle, Rx Only. Manufactured by Bausch & Lomb Incorporated Tampa, FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb, Inc.
FDA (openFDA drug enforcement)
Reported Aug 26, 2015
Medline Electrical Clipper with Charging base The Electrical Surgical Clipper is intended for the removal of body hair…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
buPROPion Hydrochloride Extended-¿release Tablets USP (SR), 200 mg, Twice-A-Day, Rx Only, 60 count Bottle, Distributed…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sun Pharma Global Fze
FDA (openFDA drug enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2015
biotene Gentle Mint Gel, 4.5 oz.(127.6 g) tubes, Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GlaxoSmithkline Consmer Healthcare
7 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 19, 2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Methotrexate Injection, USP 50 mg/2 mL (25 mg/mL), 2 mL Single-dose Vial, packaged in 5 x 2 mL vials per carton, Rx…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mylan Institutional LLC
1 more product in this recall
FDA (openFDA drug 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.