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 Feb 1, 2023
Metoprolol Succinate Extended-Release Tablets, USP 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: Alkem…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 1, 2023
Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator (racephedrine, USP 11.25), 30x0.5 mL Sterile Vials each…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nephron Sc Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 1, 2023
Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Feb 1, 2023
Epinephrine (L-Adrenaline), USP, CAS 51-43-4, 1 KG amber glass bottle in a vacuum sealed pouch, Rx only, Repackaged by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spectrum Laboratory Products, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2023
Rasagiline Mesylate Tablets 1 mg; 30 tablets in HDPE bottle; Rx only; NDC 67877-260-30; Manufactured by Alkem…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Jan 25, 2023
Orefresco Pasta Manicotti Net Wt. 10lbs. 3 oz. Keep Frozen 70019O UPC 048200237727 Caesar's Pasta Manicotti Net Wt.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caesar's Pasta, LLC
FDA (openFDA food enforcement)
Reported Jan 25, 2023
Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Macleods Pharma USA, Inc.
FDA (openFDA drug enforcement)
Reported Jan 25, 2023
R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control, REF 3D501, containing 10 x 2.0mL Control N;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.R & D Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5cm, Straight…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LP
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor. PN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
BECKMAN COULTER IRISpec CA/CB/CC control, REF 900-7211, For in vitro diagnostic use only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aurolife Pharma, LLC
FDA (openFDA drug enforcement)
Reported Dec 28, 2022
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allison Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Oncentra Brachy radiation therapy planning system software.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Unity Total Knee System. Used for knee prosthesis in total knee replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corin Ltd.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Hamilton-C6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
11 more products in this recall
FDA (openFDA food enforcement)
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Other states
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.