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 Mar 29, 2017
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Mar 22, 2017
VITROS Chemistry Products Li (Lithium) Slides, REF/Catalog Number/Product Code 1632660 (18 slide format, 90 slides per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Mar 22, 2017
The Sweet Dessert Corp., Cheesecake Cherry, Peso Neto (Net Weight) 3oz and 4 oz., Carr. 173 Km 7.1 Bo. Sumidero, Aguas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sweets & Desserts, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 15, 2017
AngioJet¿ Ultra 5000 A Console:Foot Switch Material number (U PN) 105650 Cardiovascular: The Console is a multiple-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Mar 15, 2017
ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG method is an in vitro…
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 Mar 15, 2017
Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Mar 15, 2017
Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Alfuzosin Hydrochloride Extended-release Tablets, 10 mg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sun Pharmaceutical Industries, Inc.
FDA (openFDA drug enforcement)
Reported Mar 8, 2017
EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI…
High riskUsing this product could cause serious injury, illness or death — stop using it now.United Exchange Corporation
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Mar 1, 2017
Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar. Sterile. Rx Distributed by Cardinal Health, USA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Degania Silicone, Ltd.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc., A Pfizer Company
FDA (openFDA drug enforcement)
Reported Mar 1, 2017
Procesadora La Hacienda, Inc. Recalls Meat Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Procesadora La Hacienda, Inc.
USDA FSIS
Reported Mar 1, 2017
Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 1 patch per pouch (NDC 66758-208-58), packaged in 4-count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz Inc.
FDA (openFDA drug enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accord Healthcare, Inc.
FDA (openFDA drug enforcement)
Reported Feb 22, 2017
STERRAD NX Sterilization System, Product Code: 10033, 10033-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported Feb 22, 2017
BrightView XCT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Pizza Hut Creamy Alfredo sauce, case size 40 lbs. 8 bags per case. Bags are each 80 oz (5 lbs) of sauce
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Yum Retaurants International
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Carestream DRX-Revolution Mobile X-Ray System, Model DRXR-1, Catalog No. 1019397 (all other countries), Catalog No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health 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.