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 48,100 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Feb 15, 2017
Century Packing Corp. Recalls Chicken Sausage Products Due To Misbranding
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Century Packing Corp.
USDA FSIS
Reported Feb 15, 2017
LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is used in various areas of the hospital such as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2017
Promote with Fiber Vanilla, 8oz metal can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Nutrition
5 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 8, 2017
Endure 400 Scrub-Stat (chlorhexidine gluconate) Foam Forming Solution, 4%, packaged in plastic (HDPE) bottles,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ecolab, Inc.
FDA (openFDA drug enforcement)
Reported Feb 8, 2017
MIDAZOLAM INJECTION, USP, *25 mg/5 mL, (5 mg/ mL), 5 mL vials, 10 Vials per carton, Rx only, APP Pharmaceuticals, LLC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
FDA (openFDA drug enforcement)
Reported Feb 8, 2017
Vintners Path Chardonnay Seasons Greetings Basket #795
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
30 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 8, 2017
Medtronic Strata II / Strata NSC Valves (includes Burr Hole and Lumbar Peritoneal. All Catalog Numbers. Strata-type…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Atrium Medical Ocean Drains as follows: 2002-000 Ocean single drain, with in-line connectors and suction control…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
9 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Hitachi Oasis MRI System - C-Spine Coil
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Cobas b 123 POC system The cobas b 123 POC system is a fully automated POC system for whole blood in vitro measurement…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in a 100 mL bottle, Rx only, Manufactured for: TEVA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Feb 1, 2017
Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dicom Grid Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Pentasa (mesalamine) Controlled-Release Capsules, 250 mg, 240 count bottle, Rx only, Manufactured for Shire US Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Shire PLC
FDA (openFDA drug enforcement)
Reported Jan 25, 2017
Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Jan 18, 2017
UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304
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 Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Amplia MRI" CRT -D SureScan", Amplia MRI" Quad CRT -D SureScan", Claria MRI" CRT -D SureScan", Claria MRI" Quad CRT -D…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
REFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,. Memphis, TN 38116
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2017
Label reads in part as: "Ced¿ Pud¿n***Keep Refrigerated***NET WT 20 OZ (566 g)***Manufactured and Packed by Elmec…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elmec Industries, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals…
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)
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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.