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 May 27, 2026

Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400…

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

Llorens Pharmaceuticals International Division, Inc.

FDA (openFDA food enforcement)

Food

Reported May 27, 2026

Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm…

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

Wellnov Supplements LLC

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 20, 2026

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…

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

Dexcom, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 13, 2026

ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…

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

Erbe Medical, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…

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

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…

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

Clinical Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Heraeus, PALAMIX uno. Material Number: 66057893.

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

Heraeus Medical GmbH (Dental Division)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2026

Access Total T4 Calibrator, Catalog No. 33805

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 29, 2026

Kirkland Signature Traditional Madeleines 12 Count/net wt. 18oz., Item #2000012, UPC 000020000127. Plastic clamshell…

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

Costco Wholesale Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Apr 29, 2026

Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71

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

Micro-X Ltd.

FDA (openFDA device enforcement)

Drugs

Reported Apr 29, 2026

Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister…

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

Teva Pharmaceuticals USA, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 15, 2026

0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only,…

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

Fresenius Kabi USA, LLC

13 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 15, 2026

NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2.…

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

Medline Industries, LP

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Apr 15, 2026

Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharmaceuticals USA,…

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

Teva Pharmaceuticals USA, Inc.

4 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 8, 2026

SIGNA Premier systems

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

GE Healthcare LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

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

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use

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

Erbe USA Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Apr 1, 2026

Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium…

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

Radnostix

FDA (openFDA drug enforcement)

Drugs

Reported Mar 25, 2026

Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive,…

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

Cardinal Health 200, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima…

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

Hologic, 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.