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 Dec 11, 2013
TB-0545PC: THUNDERBEAT 5 mm , 45 em, Pistol Grip TB-0535PC: THUNDERBEAT 5 mm, 35 em, Pi stol Grip TB-0545IC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus America Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2013
C-Series: Clinac, Trilogy, Trilogy Tx. , Novalis high energy linear accelerators and UNIQUE single energy linear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2013
Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2013
PACLITAXEL INJECTION, USP (semisynthetic); 300 mg/50 mL; (6 mg/mL); Multiple Dose Vial;(NDC 63323-763-50); Rx Only;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Fresenius Kabi USA, LLC
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
7 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 4, 2013
LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split Tip Driver - Short ("Driver"). Model Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lanx, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2013
MAS Urinalysis Control Level 1, Multi-analyte control (Assayed and Unassayed), Catalog/Part Numbers: 024222; Product is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Thermofisher Scientive
FDA (openFDA device enforcement)
Reported Nov 27, 2013
BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ebi, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2013
GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greenstone LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Scalp Oil), 118.28 mL (4 Fl. oz.) bottle, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hill Dermaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 27, 2013
Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
36 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Sterrad 100NX, Product Code: 10104. Used to sterilize heat and moisture sensitive reusable medical devices.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Medtronic RestoreUltra, model 37712, and RestoreSensor, model 37714, Multi-program Rechargeable Neurostimulator for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS, item #18010, Net Wt. 1 lb (454g), UPC 720056180104; item…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Priester Pecan Company, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 20, 2013
Spacelabs Healthcare elance Vital Signs Monitor, Model 93300, with Option S. It is a patient monitor with arrhythmia…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 20, 2013
VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys Heritage Hip System Revision Femoral Stems.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Prolia (denosumab) Injection, 60 mg/mL, 1 x 60 mg Single Use Prefilled Syringe per carton, Rx only, Manufactured by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amgen, Inc.
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
UniCel DxH 800 and DxH 600 Coulter Cellular Analysis Systems The UniCel DxH 800/DxH 600 analyzers are quantitative,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
HAMILTON-C2 Ventilator: Manufactured by Hamilton Medical AG CH-7402 Bonaduz, Switzerland; Imported and distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Patient Cart used in conjunction with the da Vinci S surgical and SI System. Intuitive Surgical 1266 Kifer Road…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
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.