All recall categories

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.

Medical devices

Reported Dec 6, 2023

ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 29, 2023

ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

ActiPharma, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

Achieva 1.5T

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Biomedical Division

FDA (openFDA device enforcement)

Drugs

Reported Nov 22, 2023

DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers, Original, 4FL OZ (118 ml) bottle, Hecho en Puerto…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Omega & Delta Co., Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Nov 15, 2023

Extended Phenytoin Sodium Capsules, USP, 100 mg, 100-count bottle, Distributed by Amneal Pharmaceuticals LLC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amneal Pharmaceuticals

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

DJO EMPOWR Knee Punch Handle, REF: 801-05-040

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Nov 15, 2023

4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5mEq/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Pfizer Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 15, 2023

BV Endura, BV Pulsera Philips Image Guided Therapy-Systems (IGTS)Mobile Surgery C-arm systems.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

WANABANA APPLE CINNAMON FRUIT PUREE, Net Weight: 2.50 oz (71g) Pouches, 15 poches per carton, 3-pack carton in one box.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wanabana USA LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 8, 2023

Nova Biomedical Prime Plus Analyzer -Intended to measure certain gases in blood, serum, plasma or pH of blood, serum,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nova Biomedical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number: RX4040

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Randox Laboratories Ltd.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Orgain

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Astral 100 and Astral 150 ventilators

High riskUsing this product could cause serious injury, illness or death — stop using it now.

ResMed Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 25, 2023

Kraft Singles American Pasteurized Prepared Cheese product, 24 individually wrapped slices in flexible film per pack,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Heinz

FDA (openFDA food enforcement)

Drugs

Reported Oct 25, 2023

Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in USA, NDC#…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

KVK-Tech, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 18, 2023

Constellation Vision System, REF: 8065751150

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 18, 2023

QUAKER PANCAKES WITH WHOLE GRAIN OATS, NET WT 15.97OZ (1LB)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Comercializadora Pepsico Mexico,

FDA (openFDA food enforcement)

Food

Reported Oct 18, 2023

LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Little Oak Company Ltd.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 11, 2023

Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device 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.