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 25, 2020
Stryker, REF: 0250070460, 5.0 mm x 32 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2020
Bekyree (desogestrel and ethinyl estradiol tablets USP, 0.15 mg/0.02 mg and ethinyl estradiol tablets USP, 0.01 mg),…
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 Mar 11, 2020
Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2020
CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Alprostadil/Papaverine Hydrochloride/Phentolamine Mesylate/Atropine Sulfate Injection, 18 mcg/1.8mg/0.2mg/0.02mg/mL,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
62 more products in this recall
FDA (openFDA drug enforcement)
Reported Mar 11, 2020
bellavista 1000 ventilator, Catalog number 301.100.030. bellavista is an electronically controlled pneumatic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vyaire Medical
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Akorn, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Mar 4, 2020
Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breas Medical, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Foodservice item, Norpac Catalog Number 08099, frozen FLAV-R-PAC Roasted Spicy Potatoes O'brien, 6/40 oz. (2.5 lbs.)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.PNW Veg Co. LLC
FDA (openFDA food enforcement)
Reported Mar 4, 2020
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 0 and 8 90523 00084 3
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salud Natural Entrepreneur, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 26, 2020
TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: A fixation device intended to provide secure attachment of soft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL dropper bottle, Rx only, HI-TECH PHARMACAL CO., INC.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Akorn Inc.
FDA (openFDA drug enforcement)
Reported Feb 19, 2020
The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL), 2 mL Single-dose Vial, Each Tray contains 25 Vials,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 19, 2020
Lamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutical Industries Ltd. Haifa Bay,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taro Pharmaceuticals U.S.A., Inc.
FDA (openFDA drug enforcement)
Reported Feb 12, 2020
Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
AAMI 3 FABRIC REINFORCEDGown 2XL NS, Item Code 9571NA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
38 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Granuts BBQ Mix, Net Wt/Cont. Neto 16.93 oz (480g), Contains 12 units x 1.41 oz (40g) ea. and Net Wt/Cont. Neto 6.35 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compania Nacional de Chocolates DCR S.A.
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Bentson PTFE Wire Guide, Guidewire, Global Product Number G14589, G14590
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
19 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Coated VICRYL (Polyglactin 910) Suture, 18" (45cm) Product Code J497H. The device is a synthetic absorbable sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Puerto Rico recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.