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 Nov 19, 2014
MX 16-slice CT Scanner System and MX 16-slice CT Scanner System Phase 11 can be used as a whole body computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Nov 19, 2014
Artis zeego systems, model number 10280959, with serial numbers 1000-1599 : Artis zeego is a dedicated angiography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Baxter 2B8011 Empty INTRA VIA Container with PVC Ports, Sterile fluid path, 150 ml, Admixture Products and Accessories.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Access 2 Immunoassay Systems, Catalog No. 81600N, 386220, Instructions for Use Part No. B14253A. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 12, 2014
TORISEL Kit (temsirolimus) injection, 25 mg/mL, 1 vial of TORISEL 25 mg/mL and 1 vial of 2.2 mL DILUENT per carton, Rx…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Nov 12, 2014
Siemens Calibrator E; SMN 10309079 (2 pack), SMN 10321075 (6 pack), SMN 10335532 (6 pack Ref)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, 30-count bottles and 90-count bottles, RX only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sun Pharma Global Inc.
FDA (openFDA drug enforcement)
Reported Nov 5, 2014
DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4";…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Briggs Medical Service Company d.b.a. Mabis
FDA (openFDA device enforcement)
Reported Nov 5, 2014
CUBICIN (daptomycin for injection) 500 mg, For Intravenous Use Only, Rx Only, Single use Vial, Manufactured for: Cubist…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cubist Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Nov 5, 2014
Emtriva (emtricitabine) Oral Solution, 10 mg/mL, 170 mL bottles, Rx only, Manufactured for Gilead Sciences, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gilead Sciences, Inc.
FDA (openFDA drug enforcement)
Reported Nov 5, 2014
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE Tablets, (CII),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Oct 29, 2014
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific CRM Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Bystolic (nebivolol) tablets, 20 mg/tablet, packaged as 7 tablets/bottle/carton, and 12 bottles/trays, Professional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Forest Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Oct 29, 2014
Symbia E is a multi-purpose SPECT system ideal for hospitals and outpatient centers. It is used to detect or image the…
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 Oct 22, 2014
15 L Cycler Drainage Bag Product Usage: For use with Baxter Cycler Tubing sets as a peritoneal dialysis accessory.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2014
VITROS 4600 Chemistry System (VITROS 5,1 FS System family member), System Product Code 6802445. The VITROS 4600…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Omni Micro-electrode/reference electrode for cobas b221 analyzer. The Roche Diagnostics Omni S Analyzer is a fully…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Ketorolac Tromethamine INJECTION, USP, 30 mg per mL, a) 1 mL vial (NDC 25021-701-01) b) 2 mL vial (NDC 25021-701-02),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sagent Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Oct 22, 2014
External power supply adaptors that accompany Clinitek Status+ The Clinitek Status systems is a urine analyzer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Hydrocortisone Butyrate Cream 0.1%, Net Wt. 15 gm tubes, Rx only, Manufactured for: Rouses Point Pharmaceuticals, LLC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Valeant Pharmaceuticals International
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 15, 2014
GE Healthcare Carescape Patient Data Module
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 15, 2014
RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Product Usage: RENASYS EZ and RENASYS EZ Plus Canisters are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2014
METOCLOPRAMIDE ORAL SOLUTION, USP 5 mg/5 mL, (present as the hydrochloride), 10 mL cups, Rx only. Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
FDA (openFDA drug 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.