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 Jun 26, 2013
VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog# 6802002. Used to quantitatively measure total…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Jun 26, 2013
Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 12 Digit P/N): 85008 (85008) 1053613…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
VECURONIUM Bromide for Injection, 10 mg* per vial, *1 mg per mL when reconstituted to 10 mL, for IV single use only, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sagent Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jun 19, 2013
STAR S3 ActiveTrack Excimer System (STAR S3) Mfg by AMO Manufacturing USA, LLC 510 cottonwood Drive Milpitas, CA 95035…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical Optics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 19, 2013
ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister pack with Tyvek lid. The ECHELON and ECHELON…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green & Blue Boxes,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.OLAAX International
FDA (openFDA drug enforcement)
Reported Jun 19, 2013
Cefazolin, injection, 1 gram per vial, 25 vials per box, sterile, Rx only, single-use vial, Manufactured in Austria by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz Incorporated
FDA (openFDA drug enforcement)
Reported Jun 12, 2013
Digitex Absorbable Polydiaxanone Suture, Size 2-0. Catalog Number / Code of product: 52031, 5203101400. The Digitex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Jun 12, 2013
Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 12, 2013
Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maytex Corp.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
The Zimmer Air Dermatome, REF 00- 8801- 001- 00 , Rx, non-sterile grafting instruments intended to provide variable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated for use when additional flexibility is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nephron Pharmaceuticals Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
PTS PANELS, Glucose Test Strips for use with CardioChek Brand Analyzers Product Usage: used by healthcare professionals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
LATITUDE¿ Patient Management System, Model 6488, Version 7.3. The LATITUDE Patient Management system is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific CRM Corp.
FDA (openFDA device enforcement)
Reported May 29, 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.King Legacy, a wholly owned subsidiary
10 more products in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2013
Levothroid (levothyroxine sodium tablets, USP) , 50 mcg, RX only, 100 tablets per bottle, Manufactured for Forest…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lloyd Inc.
19 more products in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2013
MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Information Technology, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
VITROS Immunodiagnostic Products CK-MB Calibrators, REF 128 6293, IVD, Ortho-Clinical Diagnostics High Wycombe HP12…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported May 29, 2013
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) 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.