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 Sep 26, 2012
A mobile, electro-hydraulically operated, fluoroscopic/C-Arm compatible general surgical table. Product Usage: Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
"Tres Monjitas***Pineapple and guava beverage***Distribuido por Vaquer¿a Tres Monjitas Inc***" Package sizes: gallons,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vaqueria Tres Monjitas, Inc.
FDA (openFDA food enforcement)
Reported Sep 19, 2012
Sterile Empty Vial and Injector (30mL PCA vial), Rx only, One/List No. 6021-03, Hospira, Inc., Lake Forest, IL 60045.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira, Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Tip Cover for 8mm Monopolar Curved Scissors (Hot Shears)Accessory, Disposable, 8mm MCS, Box of 10. The intended use of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A, M3536J, M3536M, M3536MC, M3536M1, M3536M2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
VersaTREK Windows Software, Version 5.4.3 is a component of the VersaTrek System. The Software CD will be individually…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Trek Diagnostic Systems
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Eon (Model 3716) IPG is a dual channel; 8-contact receiver designed to be connected to 4, 8, or 16 electrode leads or a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Neuromodulation Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2012
CIDEX OPA, High Level Disinfectant Solution, Glutaraldehyde-free (0.55% ortho-phthaladehyde) solution. The CIDEX OPA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Capex Shampoo (fluocinolone acetonide), Topical Shampoo, 0.01%, Rx only, For Topical Use Only, 4 fl oz in a 6 oz…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Galderma Laboratories, LP
FDA (openFDA drug enforcement)
Reported Sep 5, 2012
V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. d.b.a. Mindray North America
FDA (openFDA device enforcement)
Reported Sep 5, 2012
DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Electrode Kits (containing DGPHP RFA High-Power single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Aug 29, 2012
OPTETRAK LOGIC Proximal Tibial Spacer & Screws (2) 2.5 LT BLUE Size 2.5, 8mm***STERILE***Match insert/spacer/tray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Morton, Sodium Chloride, USP, Granular, packaged in kraft paper bags, fiber drums, and semi-bulk bags. Product is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Morton Salt Co.
FDA (openFDA drug enforcement)
Reported Aug 29, 2012
Daytrana (methylphenidate) transdermal system patch, Delivers 20 mg over 9 hours (2.2 mg/hr), 1 patch per pouch,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noven Pharmaceuticals, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 29, 2012
Mercaptopurine Tablets, USP, 50 mg, packaged in a) 60-count tablets per bottle (NDC 49884-922-02) and b) 250-count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prometheus Laboratories Inc.
FDA (openFDA drug enforcement)
Reported Aug 29, 2012
Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 22, 2012
Carboplatin Injection, 10 mg/mL, a) 5 mL multi-dose vials (NDC 61703-339-18) (NDC 61703-360-18, NOVAPLUS), b) 45 mL…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Aug 15, 2012
"***Tres Monjitas***Tropical Splash***Guanabana***15 oz***"
High riskUsing this product could cause serious injury, illness or death — stop using it now.Altura Food, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2012
AUTOMIX High Speed Compounder System, product 2M8077; automated nutrition compounders; Product Usage: The Automix…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Albuterol Sulfate Inhalation Solution, 0.083%, 2.5 mg/3 mL Sterile Unit-Dose Vials, 60-count (60 x 3 mL Sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nephron Pharmaceuticals Corp.
FDA (openFDA drug enforcement)
Reported Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 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.