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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.

Meat & poultry

Reported Jul 30, 2022

Rachael’s Food Corporation Recalls Ready-To-Eat Meat and Poultry Wrap Products Due to Possible Listeria Contamination

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

Rachael's Food Corporation

USDA FSIS

Medical devices

Reported Jul 27, 2022

Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with…

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

Baxter Healthcare Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…

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

Cordis US Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

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

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC,…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Ventana HE 600 System, automated slide preparer, for use in laboratories.

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

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

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

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

MassCheck Amino Acid, Acylcarnitines Dried Blood Spot Control Level I

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

Chromsystems Instruments & Chemicals GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

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

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP…

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

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 6, 2022

PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWAGANDHA PER 12 FL OZ STRAWBERRY CUCUMBER FLAVORED SPARKLING…

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

Independent Beverage Company LLC

FDA (openFDA food enforcement)

Food

Reported Jul 6, 2022

Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz. packed in clear plastic non-flexible package UPC 0 74641 00044 6…

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

Stellex/CF Houston, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 6, 2022

Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797

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

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the…

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

Wright Medical Technology, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear…

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

Albertsons Companies LLC

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 29, 2022

BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high…

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

Beaver Visitec International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 29, 2022

Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A

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

New Standard Device Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By:…

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

Taylor Farms Retail Inc.

FDA (openFDA food enforcement)

Food

Reported Jun 22, 2022

Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD, Item 49380. Sample Jars are 8 oz. and l lb. sized. White…

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

Butter Buds Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 22, 2022

Drager SafeStar 55, Catalog No. MP01790

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 22, 2022

illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx

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

Illumina, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 22, 2022

Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

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.