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.
2,552 stored notices name Puerto Rico, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
In the agency's Nov 11, 2026 enforcement report
Nextseq 550Dx Instrument REF: 20005715, FOR IN VITRO DIAGNOSTIC USE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
2 more products in this recall
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
ParaBien Al Grano with UPC: 0 21425 01513 4
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pan Pepin, Inc.
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
Tandem Mobi Insulin Pump, Models: 1004004, 1010750, 1012676, 1012719, 1013655, 1013656, 1013501, 1013700, 1014081,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (weekly enforcement report)
Reported Oct 28, 2026Updated Nov 2, 2026
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/SWAN/1RO/105; Material Number: M001195290
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Cork, Ltd.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI TINED 978A128 LEAD 978A133 ISTM MICRO…
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 Oct 28, 2026Updated Nov 2, 2026
Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 100 tablet bottle, Rx only, Distributed by Pfizer Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Xact mole marker for mammography Model/Catalog Number: M15RM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Solstice Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
VOCSN (Japan) Model Number: PRT-01100-100, Package PN:PRT-01126-100. used for ventilatory support.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ventec Life Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513
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 Oct 21, 2026Updated Nov 2, 2026
Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Healthmark Industries Co., Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Holsum Spinach Flour Tortillas Large, 8 count (20 oz.) UPC: 810023430629
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Holsum De Puerto Rico, Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
FoodReported Oct 13, 2026Updated Nov 3, 2026
Pan Pepín Inc. Emite Alerta por Alérgenos en el Producto Parabien al Grano Debido a la Presencia de Sésamo No Declarado
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Pan Pepín Inc. Emite Alerta por Alérgenos en el Producto Parabien al Grano Debido a la Presencia de Sésamo No Declarado
FDA (recalls & safety alerts)
FoodReported Oct 13, 2026
Pan Pepin Inc. Issues Allergy Alert of Para Bien Al Grano Due to Undeclared Sesame
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Pan Pepin Inc.
FDA (recalls & safety alerts)
Reported Oct 7, 2026Updated Oct 13, 2026
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Computed Tomography X-ray System, Model: uCT 530 with software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Criticare Technologies, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, 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.