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 Oct 9, 2019
Losartan Potassium Tablets, USP 50mg, 1000 tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Lidocaine Hydroclhoride Jelly USP, 2%, 30 mL tubes, Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
FDA (openFDA drug enforcement)
Reported Oct 2, 2019
Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 2, 2019
DigitalDiagnost C50, Stationary X-ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2019
MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sentinel CH SpA
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2019
Coconut Macaroons "Besitos de Coco" packaged in 6 oz. clamshell containers with brand name La Orocovena Biscuit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.La Orocovena Biscuit de PR, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2019
Ore Ida Spud Bites, packaged in 5lb. plain poly foodservice bags, six bags per case, frozen, Case UPC: 1 00 72714 00093…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA
FDA (openFDA food enforcement)
Reported Sep 25, 2019
Anagrelide Capsules, USP, 0.5 mg, 100-count bottle, Rx only, Manufactured in India for: Torrent Pharma Inc., Basking…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
FDA (openFDA drug enforcement)
Reported Sep 25, 2019
Oxcarbazepine Oral Suspension, USP, 300 mg/5 mL, 250 mL per bottle, Rx Only, Distr. by: West-Ward…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-Ward Columbus Inc.
FDA (openFDA drug enforcement)
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2019
Bevacizumab, 2.5 mg/0.1 mL, Norm-Ject Syringe Intravitreal Injection, Single use only, Rx only, Repackaged by AmEx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacifico National, Inc. dba AmEx Pharmacy
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 18, 2019
Bacteriostatic Water for Injection, USP, 30 mL vials, Rx only, Mfd. for: Hospira, Inc., Lake Forest, IL 60045 USA. NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Sep 18, 2019
Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Communications
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2019
TransWarmer Warming Infant Transport Mattress, Model no. 20421 Product Usage: The TransWarmer¿ Warming Infant Transport…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2019
DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant flow without impeding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leventon S. A. U.
FDA (openFDA device enforcement)
Reported Sep 4, 2019
RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Sep 4, 2019
Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190
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 Aug 28, 2019
Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, packaged in a) 0.5 FL OZ (15…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtech Products, Inc.
13 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 28, 2019
TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TiSport, LLC
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Nitrofurantoin Monohydrate/Macrycrystals Capsules, 100 mg, 100-count bottle, Rx Only, Distributed by: Alvogen, Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alvogen, Inc.
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.