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 20, 2022
CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Eszopiclone Tablets, USP 1 mg, packaged in 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Macleods Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Jul 13, 2022
OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis, sized for children and adolescents.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jul 13, 2022
ABL800 Flex Analyzer Model Numbers 393-800 and 393-801
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Jul 6, 2022
Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Volcano Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 29, 2022
Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sun Pharmaceutical Industries Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 22, 2022
Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 22, 2022
Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2022
Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TJX Companies, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
Resin UPDATE CD-ROM, REF: 250-3020 inside VARIANTnbs Sickle Cell Program Reorder Pack, REF: 250-3000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2022
DYNEX Agility, Agility Analyzer, Model No. 67000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dynex Technologies, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2022
VESSEL SEALER EXTEND, Single-Use Instrument EndoWrist Instruments 8mm, da Vinci X' da Vinci Xi', REF 480422
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Tereos Wheat Gluten, Net Weight 50 lbs, Distributed by Meelunie, Produced in France
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Able Sales Company, Inc.
FDA (openFDA food enforcement)
Reported Jun 1, 2022
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
QM-4 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 300 mcg/mL Atropine 0.2 mg/mL, Multi-Dose 10 mL vial, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympia Compounding Pharmacy dba Olympia Pharmacy
52 more products in this recall
FDA (openFDA drug enforcement)
Reported May 25, 2022
Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Vascular
FDA (openFDA device enforcement)
Reported May 25, 2022
CAIRE FreeStyle Comfort Portable Oxygen Concentrator with autoSAT, UltraSense and autoDOSE, model #AS200-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caire, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
GaviLyte -C (Polyethylene Glycol 3350, 240 g) and electrolytes for Oral Solution, USP with flavor pack NDC# 43386-060-19
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported May 25, 2022
Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of…
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 May 25, 2022
CK MB Calibrator, Catalogue Number CK2393
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported May 18, 2022
SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fagron, Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported May 18, 2022
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
1 more product in this recall
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.