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.
Reported Sep 4, 2013
Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Double Dispense with software versions 3.5.1 and 3.6.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers, Catalog Numbers LKPS1, LKPS5 and LKPTS1(D); and in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2013
Medtronic MiniMed Paradigm Reservoirs, Model No: MMT-326A (1.8mL) and MMT-332A (3.0mL) The model MMT-326A and MMT-332A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
FDA (openFDA device enforcement)
Reported Aug 28, 2013
Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography X-Ray System Product Usage: MobileDiagnost wDR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2013
C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2013
epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing of samples for pH, pCO2, pO2, Sodium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epocal
FDA (openFDA device enforcement)
Reported Aug 21, 2013
"***Gasco Golden Egg Yellow Shade Liquid***" 32 oz plastic bottles & 15 gallon drums
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gasco Industrial
FDA (openFDA food enforcement)
Reported Aug 21, 2013
Clobetasol Propionate Cream, USP, 0.05%, 15 grams, Rx only, Hi-Tech PHARMACAL label, Hi-Tech Pharmacal, Co., Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., Inc.
FDA (openFDA drug enforcement)
Reported Aug 21, 2013
Tray Surgical, ENT (various instrument trays) Used for stot age and transportation of reusable surgical instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2013
Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Aug 21, 2013
ADVIA Centaur Calibrator A. Cat. #04800735, SMN 10285904 (6 pack); Cat. # 04800840, SMN 10285905 (6 pack - REF). For…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2013
Siemens AXIOM Artis zeego x-ray, angiographic system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
BuPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, 30-count tablets per bottle, Rx only, Distributed by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis Inc.
FDA (openFDA drug enforcement)
Reported Aug 14, 2013
Enterprise 8000 Bed; an AC-powered adjustable hospital bed; ArjoHuntleigh AB, Eslov, Sweden; Models 8000, 8001, 8002,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
MERREM I.V. (meropenem for injection), 1 g meropenem equivalent, 30 mL vial, Rx only, Mfd for: AstraZeneca…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AstraZeneca Pharmaceuticals LP
FDA (openFDA drug enforcement)
Reported Aug 14, 2013
Beckman Coulter AU5800 Clinical Chemistry Analyzer, All Serial Numbers. An automated chemistry analyzer that measures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cordis Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
List No. 14200-28; SECONDARY BLOOD SET; 200 Micron Filter, 36 Inch, Non-DEHP; For Blood Product Administration; Made in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Excedrin Extra Strength (Acetaminophen 250 mg, Aspirin (NSAID) 250 mg and Caffeine 65 mg), a) 2-ct tablets in pouches…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novartis Consumer Health
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 14, 2013
Drill Guide - Chameleon FacetFuse Fixation System, Model: 11-00028 Rev. A FacetFuse Drill Guides were designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SpineFrontier, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Terazosin Hydrochloride Capsules,10 mg, 100-count bottle, Rx only, Manufactured for Teva Pharmaceuticals USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 7, 2013
DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5% Dextrose, 5000 mL container, Rx only, Baxter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA drug enforcement)
Reported Aug 7, 2013
Eon Mini - 3788 (IPG), Eon Mini system is indicated as an aid in the management of chronic intractable pain of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Endopath Electrosurgery Probe Plus II, twelve (12) different devices, including hooks, spatulas, right angles, curved…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
3 more products in this recall
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.