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 Jan 26, 2022
1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported Jan 19, 2022
Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ohio Medical Corporation
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 5, 2022
Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jan 5, 2022
Model B35200 - Percept PC BrainSense Implantable Neurostimulator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Leica Microsystems M220 F12 Microscope Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Activbody, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Kool-Aid Tropical Punch powder drink mix 19 oz. UPC 043000953501 63 oz. UPC 043000953501 82.5 oz. UPC 043000957400
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Heinz Foods Company
13 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 22, 2021
MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Dec 15, 2021
BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system. Model Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 8, 2021
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 8, 2021
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Mr. Special Jugo de Pina De Concentrado, 46 oz cans, packaged cardboard boxes 12 cans per case of 46 oz each
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Empresas La Famosa, Inc.
FDA (openFDA food enforcement)
Reported Dec 1, 2021
Medtronic CareLink SmartSync Device Manager application software (D00U005) used by the following Medtronic Cobalt and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger Kit used by the InterStim Micro (Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Healthcare Pharmaceuticals Inc.
18 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 24, 2021
BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
LEEP PRECISION Integrated System, 120V CooperSurgical part number: LP-10-120
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 17, 2021
Estradiol Valerate 20 mg/mL in Ethyl Oleate Inj. 20 mg/mL Injection in vials, Rx only, Talon Compounding Pharmacy, 2950…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vita Pharmacy, LLC dba Talon Compounding Pharmacy
129 more products in this recall
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.