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 Mar 30, 2022
Sermorelin Acetate Lyophilized powder for reconstitution, Multi-Dose 9 mg per vial, Each ML contains: 5% Mannitol USP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympia Compounding Pharmacy dba Olympia Pharmacy
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Mar 30, 2022
Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teligent Pharma, Inc.
36 more products in this recall
FDA (openFDA drug enforcement)
Reported Mar 23, 2022
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2022
BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
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 Mar 23, 2022
GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Mar 23, 2022
SAM CHEST SEAL REF CS203-EN Combo LOT Y060321-09
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sam Medical Products
FDA (openFDA device enforcement)
Reported Mar 16, 2022
CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2022
1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morton Grove Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Mar 2, 2022
DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Collagen Matrix, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2022
IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Maxi Swabstick, 3.15% w/v and 70% v/v, packaged as a) One…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Disposables International, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 23, 2022
Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion Pumps serviced…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Feb 23, 2022
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
FDA (openFDA device enforcement)
Reported Feb 16, 2022
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Premier System, nuclear magnetic resonance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
31 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 9, 2022
Baxter Spectrum IQ Infusion Pumps, Product code 3570009.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 9, 2022
ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Feb 2, 2022
GE Vscan Extend, being sold as "Vscan Extend Console"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 26, 2022
Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Multi-vessel, 6F (2.2 mm)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ev3 Inc.
1 more product 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.