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.

Medical devices

Reported Feb 3, 2021

Brain Heart Infusion Agar with 6 ug/ml Vancomycin Cat no: G14 Lot no: 472698 Manufactured: 2020-10-29 Expires:…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…

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

Respironics California, LLC

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2021

ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2021

Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…

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

Penumbra Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 20, 2021

Levetiracetam Oral Solution, 100 mg/mL, 16 fl oz (473 mL) bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY…

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

Akorn, Inc.

FDA (openFDA drug enforcement)

Food

Reported Jan 20, 2021

NETUNO Caribbean Red Snapper, Net Weight 10 Lbs (4.54 Kg), Item 101229, Product Must be Fully Cooked Prior to…

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

Netuno USA, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 20, 2021

VITROS Chemistry Products TP Slides- IVD measure total protein (TP) concentration in serum and plasma using VITROS…

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

Ortho Clinical Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…

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

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 6, 2021

Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), packaged in 2 mL Single Dose Vial, Rx only,…

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

Fresenius Kabi USA, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 30, 2020

Stimulan Kit 10cc, Model 600-010 - Product Usage: intended for use as a bone void filler for voids or gaps that are not…

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

Biocomposites, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Drugs

Reported Dec 30, 2020

Hydroxyzine Hydrochloride Oral Solution, USP (Syrup), 10 mg/5 mL, packaged in a) 4 fl oz (118 mL) bottle, NDC…

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

Morton Grove Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 23, 2020

BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of…

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

Carl Zeiss Meditec AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2020

Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF…

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

Galt Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

MAC VU360, Electrocardiograph

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

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

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Food

Reported Dec 9, 2020

Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura &…

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

Tanimura & Antle

FDA (openFDA food enforcement)

Drugs

Reported Dec 9, 2020

Anagrelide Capsules, USP 1 mg, 100 capsules, Rx only, Manufactured in India for: Torrent Pharma Inc., Basking Ridge, NJ…

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

Torrent Pharma Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Dec 2, 2020

DOXOrubicin Hydrochloride Injection, USP, 10 mg / 5 mL (2 mg / mL), 5 mL fill in a 6 mL vial, Single Dose Vial, Rx…

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

Fresenius Kabi USA, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 25, 2020

VNS Therapy¿ AspireSR¿ Generator

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…

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

Micro-Tech USA

FDA (openFDA device enforcement)

Drugs

Reported Nov 25, 2020

DCL Active Mattifying Cleanser (Salicylic Acid 2%), 125mL/4.2 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT…

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

Milbar Laboratories, Inc.

13 more products in this recall

FDA (openFDA drug 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.