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 May 22, 2019
Tissu-Trans FILTRON 100, Catalog 3-TT-FILTRON 100, sterile, disposable, one-patient use. The firm name on the label is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shippert Medical Technologies
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), 2 mL Vials, Rx only, Mfd. for Sagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sagent Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported May 15, 2019
Atellica IM 1300 Analyzer, Material Number 11066001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
G-6-PDH Deficient Control (G-6-PDH CONTROL D), Catalogue Number PD2617 Product Usage: This product is intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
Losartan Potassium Tablets, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b)1000-count (NDC: 13668-113-10) per bottle,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported May 1, 2019
Edwards Lifesciences, Fogarty Dilation Atrioseptostomy Catheter, Sterile EO, Rx Only, REF: 830705F Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2019
Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cordis Corporation
FDA (openFDA device enforcement)
Reported Apr 24, 2019
VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 4-0 UND VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton
High riskUsing this product could cause serious injury, illness or death — stop using it now.Little Red Rooster Company
FDA (openFDA food enforcement)
Reported Apr 24, 2019
Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in (a) 150 mL bottle (NDC 0093-4150-80) (b) 80 mL bottle…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Apr 17, 2019
Immunoassay Premium Controls, Model Numbers IA2633 and IA2638 Product Usage: This product is intended for in vitro…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Randox Laboratories Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
LOSARTAN POTASSIUM TABLETS, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b) 1000-count (NDC: 13668-113-10), per bottle,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 10, 2019
Abbott ARCHITECT Creatine Kinase, IVD, REF 7D63-21.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2019
CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous Autotransfusion System) is indicated for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Diclofenac Sodium Topical Solution, 1.5% w/w, 5 FL. OZ. (150 mL) bottle, Rx Only, Manufactured for: Ingenus…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ingenus Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Mar 27, 2019
Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pharmacal Co, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn Inc.
FDA (openFDA drug enforcement)
Reported Mar 27, 2019
Valsartan Tablets USP 160 mg, 100 Tablets (10 x 10) per Unit Dose Blisters, Rx Only, Packaged and Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Health Packaging
FDA (openFDA drug enforcement)
Reported Mar 27, 2019
El Rey Chocolitas 12.69oz (360gr) and 2.2lb (1 Kg)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cesar Iglesias, S.A.
FDA (openFDA food enforcement)
Reported Mar 27, 2019
Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
FDA (openFDA drug enforcement)
Reported Mar 20, 2019
Gentamicin Sulfate Ophthalmic Solution, USP, 0.3%, 5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn, Inc.
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.