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 48,123 notices were distributed nationwide, so they reach Puerto Rico too — those are in the archive.
Reported Feb 13, 2013
Taztia XT(diltiazem HCI extended release capsules, USP, Once-A-Day Dosage, 360 mg, 90 Capsules per bottle, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Watson Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Feb 13, 2013
PredniSONE Tablets, USP, 10 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1473-01), b) 1000-count tablets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-ward Pharmaceutical Corp.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 6, 2013
Alere Cholestech LDX Multianalyte Control, 2 vial set, Catalog Number: 88769 Alere Cholestech LDX Multianalyte Control…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Temodar (temozolomide) Capsule, 20 mg per capsule, 5 capsules per package, For Oral Administration, Rx Only, Cytotoxic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schering-Plough Products, LLC
FDA (openFDA drug enforcement)
Reported Feb 6, 2013
Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Jan 30, 2013
ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP, Disposable Hyfrecator(R) Tips, REF/Catalog No. 7-100-8CS, Sterile, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
19 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2013
Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***BLACK BEAR***of the BLACK FOREST*** Naturally…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Marine Harvest USA, LLC
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 30, 2013
Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 30, 2013
Lisinopril Tablets, USP 40 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1270-01); b) 1000-count tablets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-ward Pharmaceutical Corp.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 23, 2013
Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model 59051, 59081,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bausch and Lomb, Incorporated
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Spacelabs Smart Disclosure System, Model 92810, is an integrated component of the Intesys Clinical Suite (ICS) G2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valproic Acid Activity, 100-count tablets per bottle, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Upsher Smith Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Jan 16, 2013
Product labeled in part: ***PARAMOUNT RESERVE***PRODUCT OF CHILE FARM RAISED ATLANTIC SALMON PACKED BY: ALIMENTOS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Multiexport Foods, Inc.
FDA (openFDA food enforcement)
Reported Jan 16, 2013
&TRIGAL***Empanadillas de Pizza (Pizza turnovers)***12 ct***Pastry Foods Inc., Rio Piedras, PR&
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pastry Food Products Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 16, 2013
Immunoradiometric assay. Device is an immunoradiometric assay designed for the quantitative measurement of thyroid…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Synthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bottle, Rx Only, NDC 0074-7069-90; ABBOTT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA drug enforcement)
Reported Jan 9, 2013
AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cooper Vision Caribbean Corp.
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Plum A+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold under the following…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Nature's Plus GLUTEN Free SPIRU-TEIN HIGH PROTEIN ENERGY MEAL, S'mores (Flavor), 1.2 OZ. (34g) Packet, Display Box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natural Organics
FDA (openFDA food enforcement)
Reported Jan 2, 2013
Thyro-Tab 0.050 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lloyd Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 26, 2012
The Access hLH assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Nalbuphine HCl Injection, 20 mg/mL, 10 mL Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 26, 2012
Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
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.