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 Nov 18, 2015
MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Myelo-Nate CSF Sampling Kit, Neonatal/Pediatric cerebralspinal fluid sampling sterile tray, including a lumbar puncture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Utah Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
EnVision FLEX/HRP visualization reagent found in the following kits: EnVision FLEX, High pH (Link) EnVision FLEX+,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
VITROS Chemistry Products Calibrator Kit 9 Calibrator, 2 mL, Product Code 8568040, Unique Device Identifier No.…
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 Nov 4, 2015
Welch Allyn KleenSpec Corded Illumination System, Vaginal Speculum Lighting System, Model Number 78x Series…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2015
XiO Radiation Treatment Planning System. Used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2015
Metformin Hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, Rx only, Manufactured by: Actavis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Actavis Laboratories, FL, Inc.
FDA (openFDA drug enforcement)
Reported Oct 21, 2015
FUROSEMIDE Tablets USP, 20 mg, 1000-count bottle, Rx only, Boehringer Ingelheim Roxane Laboratories, Roxane…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boehringer Ingelheim Roxane Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 21, 2015
Toshiba Aquilion CT System TSX-101A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2015
Fenofibric Acid Tablets, 35 mg, 30-count bottles, labeled as a) FIBRICOR (fenofibric acid) Tablets, NDC 13310-101-07,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tribute Pharmaceuticals US Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 14, 2015
MICroSTREP plus 1 Panel, Part No. B1027-201 Product Usage: MicroScan MICroSTREP plus panels are designed for use in…
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 Oct 14, 2015
Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Oct 7, 2015
Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Inc.
FDA (openFDA drug enforcement)
Reported Oct 7, 2015
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Guthy-Renker LLC
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 7, 2015
Zimmer Guide Wires for orthopedic procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Refresh Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant Eye Ointment, packaged in a) Net wt. 0.12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergan Sales, LLC
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 30, 2015
0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG VIAFLEX Container, Single Dose Container, Rx Only, Baxter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA drug enforcement)
Reported Sep 30, 2015
MicroScan LabPro Information Manager System, Version 1.0 to Version 4.11, Catalog No. 10714149, 10714150. Intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Disposable Reflective Marker Spheres The Disposable Reflective Marker Spheres used in conjunction with a stereotaxic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, ORS-300, ORS-301,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ecolab Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufactured by: Majopa Industries…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Majopa Industries Corporation
FDA (openFDA food enforcement)
Reported Sep 23, 2015
Cevimeline Hydrochloride Capsules, 30 mg a) 100 count bottle, and b) 500 count bottle, Rx Only, Manufactured by: Apotex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Inc.
FDA (openFDA drug enforcement)
Reported Sep 23, 2015
Pointe Scientific autoHDL Reagent H7545 H7545-R1 in a bulk cube container or HDPE plastic bottle H7545-1000 kit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pointe Scientific, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
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.