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Recalls distributed in Connecticut

These notices name Connecticut 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.

3,041 stored notices name Connecticut, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

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

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…

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

Philips Respironics, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 14, 2022

Finger Roll 24-pack (033474400885))

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

Piantedosi Baking Co., Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2022

Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)

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

Saranas, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 7, 2022

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

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

Oculus Optikgeraete GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice,…

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

Woodland Foods LLC

FDA (openFDA food enforcement)

Food

Reported Sep 7, 2022

Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

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

Yem Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 31, 2022

Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Nobel Biocare N1 TiUltra TCC NP 3.5x13mm

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

Nobel Biocare

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 24, 2022

Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.

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

Myolyn Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2022

cobas e801 Immunoassay Analyzer

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2022

Xhibit Telemetry Receiver, Model: 96280

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

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

Aesculap Implant Systems LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

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

Neotract Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML…

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

North American Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software

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

St. Jude Medical, Cardiac Rhythm Management Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

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

The Procter & Gamble Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL

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

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2022

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…

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)

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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.