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 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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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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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.