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 19, 2017
Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Stat Profile Prime ABG Analyzer PN 53655 Stat Profile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Biomedical Corporation
FDA (openFDA device enforcement)
Reported Jul 19, 2017
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Finola, Style Octopus in Pickled Sauce, Product of Spain, Wild Caught, Net Weight 4.1/10oz (115g), Empacado…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bacalafoods Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Fudge Brownie Collagen Protein Bar. Each bar is packed in foil wrapper, net wt. per bar 1.58 oz (45g). There 12 bars…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bulletproof 360 Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Logic Fit Tibial Tamp Head
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Fludeoxyglucose F 18 Injection, 20mCi/mL to 200 mCi/mL at EOS, 30 mL Multiple-Dose Vial, Rx Only, Manufactured by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lantheus MI Radipharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jul 5, 2017
Access Total T3, A34435H, Catalog No. 33830
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2017
DRX-Revolution Mobile X-Ray System; MODEL DRXR-1; Catalog # 1019397 (all other countries) and Catalog 1060177 (China…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Exactech 1.5" Novation Calcar Planer Guide Tip To assist the surgeon in the implantation of Novation hip system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sanofi-Aventis U.S. LLC
FDA (openFDA drug enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Pereyra-Raz Ligature Carrier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
GE Healthcare Revolution EVO X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
16 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Pointe Scientific Hitachi Total Bilirubin Rl Reagent Product Usage: Two part Chemistry Reagent Hitachi Total Bilirubin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtest Holdings, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R, Item Number: L4; POLSORB 0 18 VIO PRECUT 226T; Item Number: L14;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Arsenal Spinal Fixation System, Set Screw, Part No. 47027 Product Usage: The Arsenal Spinal Fixation System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Oxygen Masks, Elongated (under chin), Adult Med Conc., No Tubing, Product Code 104-E;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Zenatane (isotretinoin) Capsules, USP, 10 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 7, 2017
The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Liquid Urine Control Level 3 For Professional Use in the quality control monitoring of In-Vitro Diagnostic Urinary…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Randox Laboratories
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device 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.