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 Dec 27, 2017
Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP, 90mcg/20mcg), 28 tablet dispenser (blister foil unit), Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Dec 20, 2017
LIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 20, 2017
Penicillin V Potassium for Oral Solution, USP, 125 mg (200,000 U) per 5 mL, 100 mL (when mixed) bottle, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Dec 13, 2017
Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Dec 6, 2017
Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eai-Jr286 Inc.
FDA (openFDA drug enforcement)
Reported Dec 6, 2017
ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Nov 29, 2017
Optetrak Offset Tibial Tray and Screws, Size 0F/0T, Alpha, Ref 208-04-01, Sterile, RX.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
33 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2017
Dark Chocolate Almond, 12/10 oz., 12/18 oz., 18/14 oz., 8/10 oz., 12/8 oz., 8/8 oz., 18 pc.,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GKI Foods, LLC
20 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 29, 2017
Halyard Closed Suction System for Adults with BALLARD Technology WET PAK. 12 saline vials per kit, 20 kits per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2017
Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Limited
FDA (openFDA drug enforcement)
Reported Nov 29, 2017
Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Vials (NDC 0641-6145-01), packaged in 25 x 1 mL Vials per…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.West-Ward Pharmaceuticals Corp.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 22, 2017
Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amerisource Health Services
FDA (openFDA drug enforcement)
Reported Nov 22, 2017
AQUIOS CL Flow Cytometer, Catalog No. B30166, Rx. The firm name on the label is Beckman Coulter Ireland Inc., Ireland.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Nov 22, 2017
Urin D/S Tablets Methenamine 81.6 mg, Sodium Biphosphate 40.8 mg, Phenyl Salicylate 36.2 mg, Methylene Blue 10.8 mg,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Llorens Pharmaceutical Corp.
FDA (openFDA drug enforcement)
Reported Nov 22, 2017
smith&nephew LEGION L-WEDGE, 10 MM DIS X 5 MM POS, SIZE 4, SCREW-ON FEMORAL WEDGE, REF 71421733, STERILE R Product The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2017
Trafon Group Recalls Chicken and Pork Products Produced Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Trafon Group
USDA FSIS
Reported Nov 15, 2017
AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aaren Scientific Inc.
FDA (openFDA device enforcement)
Reported Nov 8, 2017
CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., 50 mL, For use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 8, 2017
Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Nov 1, 2017
MicroPort Orthopedics SCHANZ SCREW SELF DRILL, SIZE 4mm, REF 20070057, STERILE R Product Usage: MPO Total Hip Systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroPort Orthopedics Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2017
Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex America, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2017
Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Oct 18, 2017
ARCHITECT c4000 Cuvette Segment, List number 02P75-01. The firm name on the label is Abbott Laboratories, Abbott Park,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Oct 4, 2017
Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sandoz 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.