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 Jul 21, 2021
Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Lingen Disposable Virus Sampling Kit, Item MTM-04, 40 tubes/box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mercedes Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
LeadCare II Blood Lead Test Kit Catalog Number 70-6762
High riskUsing this product could cause serious injury, illness or death — stop using it now.Magellan Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI: (01)15099590742744
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 Jun 30, 2021
Probe Cover 6" x 48" regular PE w/ 2 Elastic Bands-Ultrasonic Transducer Cover Bulk Non-sterile Item ID: A-AU-0776NA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exact Medical Manufacturing, Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
BTREX PLUS, Dietary Supplement 100 Caplets, UPC 05380930801
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lopez Gonzalez Santana Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 23, 2021
OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jun 9, 2021
Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boehringer Ingelheim Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 9, 2021
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hi Tech Pharmaceuticals
FDA (openFDA food enforcement)
Reported Jun 9, 2021
Leccurate SARS-CoV-2, Antibody Rapid Test Kit (Colloidal Gold Immunochromatography), 1 test, IVD. for qualitative…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lepu Medical Technology (beijing) Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 9, 2021
0.5% Bupivacaine Hydrochloride Injection, USP, 150 mg/30 mL (5 mg/mL), 30 mL Single-dose Teartop Vials (NDC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pfizer, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 2, 2021
Native Fluoride Toothpaste for Sensitive Teeth, with Fluoride, 5% potassium nitrate, 0.243% sodium fluoride (0.14% w/v…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accupac, Inc.
FDA (openFDA drug enforcement)
Reported Jun 2, 2021
NP Thyroid 15 Thyroid Tablets, USP 1/4 grain (15 mg), packaged in a) 100-count bottles (NDC 42192-327-01) and b)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Acella Pharmaceuticals, LLC
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 2, 2021
Access SARS-CoV-2 Antigen, REF C68668, UDI: (01)15099590742713, 3.30 mL/R1a, 4.70 mL/R1b, 4.20 mL/R1c, 3.10 mL, R1d,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jun 2, 2021
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jun 2, 2021
GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 26, 2021
BTREX PLUS, Dietary Supplement 2 Caplets, UPC 05380930802 (Physician Samples)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lopez Gonzalez Santana Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 19, 2021
AquaBplus and AquaBplus B2 Water Purification System - Product Usage: Intended for use with a hemodialysis system to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported May 19, 2021
BTREX PLUS, Dietary Supplement 100 Caplets
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lopez Gonzalez Santana Corporation
FDA (openFDA food 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.