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 Feb 24, 2016

REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2016

Actuator for angiographic x-ray monitor ceiling suspension system. Actuator short Assy: THC8AWDS-121 and Actuator long…

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2016

Eclipse Treatment Planning System versions 11, 13.0, 13.5 and 13.6; Model number: H48; Product Usage: The Eclipse…

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

Varian Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 17, 2016

Label reading in part: "CRIADA***PREMIUM GANDULES VERDES GREEN PIGEON PEAS***In water with salt*** NET WT. 15 oz…

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

A.R.Food Brokerage Corp.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 17, 2016

Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…

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

Biomet France SARL

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+,…

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

GE Medical Systems, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 17, 2016

Kraft Singles American packaged in a blue box with white lettering.

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

The Kraft Heinz Company

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 17, 2016

IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are…

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

Zimmer Dental Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2016

Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This instrument has been designed to be used…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Drugs

Reported Feb 10, 2016

Lyrica (pregabalin) capsules, 50 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer Inc.,…

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

Pfizer Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 10, 2016

Allura Xper FD10, FD10 C, and FD10 F; Model Numbers: 722026 722010 722003 722002 722001 Intended for Cardiovascular and…

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

Philips Electronics North America Corporation

28 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2016

ADVIA Centaur PSA Assay; Catalog Number: 06574155/SMN 10310292 (100 test kit) and Catalog Number: 02676506/SMN 10310293…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 3, 2016

Levofloxacin Tablets USP, 500 mg, packaged in 100-count (10 x 10) blister cards per carton, individual blisters labeled…

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

Amerisource Health Services

FDA (openFDA drug enforcement)

Drugs

Reported Feb 3, 2016

Cyclopentolate Hydrochloride Ophthalmic Solution USP, 1%, Packaged in a) 2 mL Bottles (NDC: 24208-735-01) and b) 15 mL…

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

Bausch & Lomb, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 27, 2016

Brainlab Cranial Navigation System: An Image Guided Surgery System / Stereotactic. Radiology Departments. The BrainLAB…

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

Brainlab AG

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2016

GE Healthcare, Aespire 7900, 1009-9012-000 & Aespire View, 1009-9212-000. The family of GE Datex-Ohmeda Aespire…

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

GE Medical Systems, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 27, 2016

Lindane Lotion, USP 1%, For External use Only, Rx Only, 2 fl oz (60 mL) bottle, MGP, NDC 60432-833-60

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

Morton Grove Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Jan 27, 2016

Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal Rx -- Pine Pharmaceuticals, 100 Colvin Woods…

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

Pine Pharmaceuticals, LLC

3 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 20, 2016

iChem 10 SG Urine Chemistry Strips, PN 800-7005. Intended for the in vitro measurement of glucose, protein, bilirubin,…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

0 deg, 8mm Endoscope, IS4000: Model numbers: 470026-34, 470026-40, 470026-41. General and Plastic Surgery: The da Vinci…

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The Neo-Tee T-Piece Resuscitator is a gas powered…

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

Mercury Enterprises, Inc. dba Mercury Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

VITROS 3600 Chemistry System, Catalog Number 6802783, Unique Device Identifier Number 10758750009930, Software Product…

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

Ortho-Clinical Diagnostics

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Gynecare Thermachoice III Uterine Balloon Therapy System Ethicon, Inc. The GYNECARE THERMACHOICE¿ III Uterine Balloon…

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

Ethicon, 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.