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 48,122 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.

Medical devices

Reported Feb 5, 2014

User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension Vista 1500 System with software version…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 System is intended to be used during cardiopulmonary…

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

Sorin Group Deutschland GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or…

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

Spacelabs Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

Symmetry and CODMAN brands, QUAD-LOCK Sterilization Container. Sterilization container systems manufactured and…

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

Symmetry Medical/SSI

FDA (openFDA device enforcement)

Drugs

Reported Feb 5, 2014

ROHTO Redness Relief, arctic, Redness Reliever, Lubricant Eye Drops, Sterile, Net. Wt. 0.4 FL OZ (13 mL). UPC 3 10742…

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

The Mentholatum Co.

4 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Feb 5, 2014

Pantaprazole Sodium Delayed Release Tablets , USP 40 mg, 1000 tablets bottle, Rx only. Manufactured by: Wockhardt…

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

Wockhardt USA Inc.

FDA (openFDA drug enforcement)

Meat & poultry

Reported Feb 4, 2014

Pennsylvania Firm Recalls Chicken Noodle Soup Due to Misbranding and Undeclared Allergens

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

Pennsylvania Firm

USDA FSIS

Meat & poultry

Reported Feb 4, 2014

Texas Firm Recalls Beef Products Due To Possible E. Coli Contamination

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

Texas Firm

USDA FSIS

Medical devices

Reported Jan 29, 2014

TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, one 10 mL vial of Ethiodized Oil…

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

Codman & Shurtleff, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: Precision 500D,…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 29, 2014

sertraline HCl tablets, 25 mg, 30 Tablets, Rx only, GREENSTONE BRAND --- Distributed by: Greenstone LLC, Peapack, NJ…

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

Greenstone LLC

FDA (openFDA drug enforcement)

Drugs

Reported Jan 29, 2014

HydrOXYzine HCI Tablets USP 10 mg, 100 count bottles, Rx only. Mfd by KVK-TECH, INC, Newtown, PA 18940. NDC…

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

KVK-Tech, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 29, 2014

Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The intended use of the oxygen…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

VITROS Chemistry Products COCM Reagent

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B, packaged in cartridges of 50 discs, 5…

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

Remel Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for use as an interface between a ventilator…

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

Vital Signs Colorado Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 22, 2014

0.45% Sodium Chloride Injection USP, 1000 mL. Rx only, Manufactured by B. Braun Medical Inc, 2525 McGaw Ave, Irvine, CA…

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

B. Braun Medical Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 22, 2014

Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 9-12 mm Injects Above UPN: M00547100 The Extractor Pro XL…

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

Boston Scientific Corporation

8 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 22, 2014

Quinapril Tablets USP, 5 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD…

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

Lupin Pharmaceuticals Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Jan 22, 2014

Zithromax (azithromycin for injection), 500 mg/vial, Sterile, Rx Only, For I.V. infusion only, No latex, No…

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

Pfizer Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 15, 2014

Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…

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

Ansell Sandel Medical Industries LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Puritan Bennett 840 ventilator systems software part number 4-070212-85, revision AB-AG. The intended use of the…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

The Vantage Digital Panoramic System delivers high-value features standard on every system: - Five pre-programmed exam…

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

Midmark Corp. dba Progeny 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.