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 Feb 28, 2018
Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Xpert CT/NG Catalog GXCT/NG-120 Batch 1000049568, Catalog GXCT/NG-10 Batch 1000053075, Catalog GXCT/NG-10 Batch…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Q.Care, Oral Cleansing & Suctioning System q4. Contains: 1 Covered Yankauer and Y-Connector, 2 Suction Toothbrush…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sage Products Inc.
63 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 14, 2018
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chobani
FDA (openFDA food enforcement)
Reported Feb 14, 2018
Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 15cm, Material CA15L1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Covidien Vistec" X-Ray Detectable Sponges, 7317 Vistec" X-Ray Detectable Sponges Sponge. product Usage: Vistec X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LP
FDA (openFDA device enforcement)
Reported Feb 14, 2018
TITAN, 6 rellenos, Potato Puffs with Meat Flavor, Net Weight 26.4 oz (748g)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Empresas Barsan, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 14, 2018
Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 g tubes (NDC 0713-0638-31);…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.G & W Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Feb 14, 2018
TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Feb 14, 2018
PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Panoramic Rental Corp.
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring and inspecting complete components made of plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Metrology Inc.
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution, Active Ingredient: Povidone-iodine USP 10%. Aplicare,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
67 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 7, 2018
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
FDA (openFDA device enforcement)
Reported Jan 24, 2018
ACCOLADE SR Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
23 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2018
Orange Cream Ice Cream Bars sold under the following labels: Sold in a 12-pack: Ahold UPC: 6 88267 03292 9, Econo UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fieldbrook Foods Corporation
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2018
Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthoscan, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Valsartan Tablets, USP, 160 mg, 90-count bottles, Rx Only, Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prinston Pharmaceutical Inc.
FDA (openFDA drug enforcement)
Reported Jan 3, 2018
VITROS Chemistry Products PHYT Slides, REF/CATALOG 829 8671, Rx ONLY, IVD; Ortho-Clinical Diagnostics, Inc. For in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 3, 2018
Rx series HbA1c REF/Catalog Number HA3830, GTIN 05055273203561, IVD; -- RANDOX LABORATORIES LTD. , This product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Dec 27, 2017
Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 27, 2017
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pfizer 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.