All recall categories

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.

Food

Reported Jun 8, 2016

Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Liquid Assets Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Drugs

Reported Jun 8, 2016

Ceftriaxone for Injection USP, 250 mg, Single Use Vial, packaged in a) 1-count Vials per box (NDC 68180-611-01), and b)…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Lupin Pharmaceuticals Inc.

4 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 8, 2016

Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

CADD Administration Sets with Flow Stop, Product Reorder No: 21-7321-01, 21-7321-24, 21-7322-01, 21-7322-24,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 8, 2016

Choice Products Supreme Elixir 32oz.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

World's Choice Products

2 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Jun 1, 2016

ORIS (chlorhexidine gluconate), oral rinse, 0.12%, packaged in 16 fl. oz. (473 mL) PET bottle, Rx only, Manufactured…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Akorn, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Jun 1, 2016

0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corp.

3 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 1, 2016

Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and Bottles. Catalog # M35500 (D-Vapor) and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jun 1, 2016

OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Kabi USA, LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Jun 1, 2016

Zoloft (sertraline HCl) tablets, 100 mg*, 30 count bottles, Rx only, Distributed by Roerig, Division of Pfizer, Inc.,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pfizer Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Jun 1, 2016

Amikacin Sulfate injection USP,1 gm/4 mL (250 mg/mL) 4mL vial, Rx only, Manufactured in Hungary For: Teva…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Teva Pharmaceuticals USA

FDA (openFDA drug enforcement)

Medical devices

Reported May 25, 2016

Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Diamedix Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 25, 2016

Alfalfa Sprout Product***Germinados Campo Verde***San Sebastian, Puerto Rico

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Germinados Campo Verde

FDA (openFDA food enforcement)

Drugs

Reported May 25, 2016

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hospira Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 18, 2016

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Applied Medical Resources Corp.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

NeuViz 64 Multi-Slice CT Scanner System (consist if two variants: NeuViz 64e, NeuViz 64i)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Neusoft Medical Systems Co., Ltd.

FDA (openFDA device enforcement)

Drugs

Reported May 18, 2016

Dryses Aluminum Chlorohydrate Antiperspirant Solution, 3.4 fl. oz (100 mL) bottle, over the counter, Manufactured by…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sesderma, SL

9 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported May 11, 2016

Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L Serial # >200318 and < 2039222 The Dialog+ can be…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

B Braun Medical Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 11, 2016

ALFALFA SEED, NET WT. 50 LB. International Specialty Supply LLC, Cookeville, TN

High riskUsing this product could cause serious injury, illness or death — stop using it now.

International Sprout Holding Inc.

FDA (openFDA food enforcement)

Food

Reported May 11, 2016

TRIGAL*** Empanadillas Sabor a Carne (meat flavored turnovers)***Peso neto 3 lbs (Net Weight 3 pounds)*** Pqte. de 12…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pastry Food Products Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 4, 2016

Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

NOW Foods

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2016

NeuViz 16 Multi-Slice CT Scanner System PN: 989605858501 a whole body computed tomography X-ray system featuring a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips and Neusoft Medical Systems Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2016

PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator; High pressure units (HPU) (40L and 45L).…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2016

Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

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.