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 48,123 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported May 1, 2013
NeuViz 16 Multi-Slice CT Scanner System, Part number (PN): 989605858501, Model: NeuViz 16. This is a computed X-ray,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips And Neusoft Medical Systems Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Clinical Chemistry Phenobarbital, list number 1E08
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Industries Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
GERBER¿ Pure Water (1 Plastic Gallon)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nestle Puerto Rico Inc.
FDA (openFDA food enforcement)
Reported Apr 24, 2013
VITROS 5,1 FS Chemistry System, Product Code 6801375 and VITROS 5,1 FS Chemistry System Refurbished, Product Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Levoxyl (levothyroxine sodium) tablets, USP 25 mcg, packaged in a) 100-count bottles (NDC 60793-850-01) and b)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
10 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 24, 2013
Children's Acetaminophen Oral Suspension, 650 mg/20.3 mL unit dose cup (NDC 68094-650-59), packaged in 30-count cups…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Precision Dose Inc.
FDA (openFDA drug enforcement)
Reported Apr 24, 2013
Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Precise Treatment Table. To be used as part of radiation therapy treatment process.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the determination of the activated partial thromboplastin time…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermo Fisher Scientific (Asheville) LLC
FDA (openFDA device enforcement)
Reported Apr 17, 2013
G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Animas Corporation
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiographic Balloon Catheter. The Arrow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
LEEP REDIKIT Product No. 6060 In a Loop Electrosurgical Excision Procedure, a thin, low-voltage electrified wire loop…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cooper Surgical, Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Tizanidine Tablets USP, 4 mg, 150-count tablets per bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dr. Reddy'S Laboratories
FDA (openFDA drug enforcement)
Reported Apr 10, 2013
Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is indicated for the treatment of symptoms due to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Test Strips packaged in the OC-Light Manual iFOBT Kit, Catalog No. FOB50. For the rapid, qualitative detection of human…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir, Catalog number 05232732001. Used with the cobas¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2013
Mrs. Bridges Scottish Raspberry Preserve ("Jam"); Net Wt. 42g /1.5oz; service size 15g; servings per package: 2.8; ID…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The TJX Companies, Inc.
FDA (openFDA food enforcement)
Reported Apr 3, 2013
VITEK 2 60 computer system when equipped with the following Hewlett-Packard PC models: (1) rp5700, Cat. #W0452; (2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL is an in vitro diagnostic product for the…
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 Apr 3, 2013
Siemens Axiom Artis zeego systems with software version VC14, VC20 and VC21 in conjunction with specific technical…
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)
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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.