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 Sep 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Euphora Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular Galway dba Medtronic Ireland
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Organic Coconut Sugar, 16oz bag, 12 bags/case, packed in a foil bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NOW Foods
FDA (openFDA food enforcement)
Reported Sep 13, 2017
Coulter LH 750, Coulter LH 780, and Coulter LH 500 Analyzers Hematology Analyzers are quantitative, automated…
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 Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
LX3 Floor Stand for LuxOR Ophthalmic Microscope; Endure LuxOR Q-VUE Ophthalmic Microscope. LX3 Microscope Floor Stands…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, Ltd.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morton Grove Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amgen, Inc.
FDA (openFDA drug enforcement)
Reported Aug 23, 2017
EMBLEM S-ICD, Model A209, Subcutaneous Implantable Cardioverter Defibrillator, RX. Product Usage: The S-ICD system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Plum 360 Infusion System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 16, 2017
BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 16, 2017
MCCAIN ONION RING BATTERED PORTION PERFECT ¿ 60X4 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods Canada, Inc.
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Potassium Phosphates Inj., USP, 45 mM (3 mM P/mL) Also contains: 66 mEq K+ (4.4 mEq/mL) 15 mL, Single-dose, Caution:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira a Pfizer Company
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 9, 2017
Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Threshold Enterprises Ltd.
FDA (openFDA food enforcement)
Reported Aug 2, 2017
Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2017
Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fisher Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
BRILINTA (ticagrelor) tablets, 90 mg, 8-count Professional Sample bottles, Rx only, Mfd. for: AstraZeneca…
High riskUsing this product could cause serious injury, illness or death — stop using it now.AstraZeneca Pharmaceuticals, LP
FDA (openFDA drug enforcement)
Reported Jul 19, 2017
Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
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.