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 Aug 29, 2018
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handicare USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Vision Care, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of multiple adult, pediatric and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured for:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Westminster Pharmaceuticals LLC
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 22, 2018
Improve Blood Collection Sets with Multiple Sample Luer Adapter - Sterile/EO Product Usage: The Blood Collection Set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Guangzhou Improve Medical Instruments Co., Ltd.
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Arkon Anesthesia Delivery System with Arkon Software Version 2.70, Display Unit Assembly 650-1769-00 installed, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spacelabs Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Levofloxacin Injection in 5% Dextrose, 250 mg (5 mg/mL), 250 mg in 50 mL 5% Dextrose, 50 mL Single Use Container bag,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Baxter Healthcare Corporation
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 15, 2018
Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stavis Seafoods, Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2018
AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
RITZ BITS CHEESE BIG BAG 3 Oz, Pouch Retail: 12 per case Foodservice: 36 per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Global LLC
12 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 8, 2018
Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer
FDA (openFDA drug enforcement)
Reported Aug 8, 2018
Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 400 mg in 200 mL (2 mg/mL), 200 mL Single Dose…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Renaissance Lakewood, LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 8, 2018
Potassium Citrate Extended-Release Tablets, USP, 15 mEq, 100-count bottles, Rx only, Manufactured for: Vensun…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vensun Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 1, 2018
PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 80 mg/12.5 mg tablets, 90 count-count bottle, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
8 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 25, 2018
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
FDA (openFDA device enforcement)
Reported Jul 18, 2018
Fluocinolone Acetonide Topical Solution, USP, 0.01%, 60 mL bottle, Rx Only, Manufactured by: Actavis Laboratories UT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Jul 11, 2018
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Randox Liquid Assayed Specific Protein Control - Level 1 (SP Control 1), Cat. no. PS2682
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an evacuated blood collection tube that provides a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206, Article Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiopulmonary Ag
2 more products 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.