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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.

3,077 stored notices name Connecticut, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.

Medical devices

Reported Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The…

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

THOR Photomedicine Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2025

Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2025

Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile; 2.…

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

Spiggle & Theis Mt GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray…

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

Carefree Surgical Specialties

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2025

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 20, 2025

Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069,…

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Aug 20, 2025

High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C

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

Merit Medical Systems, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2025

Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A…

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

Thoratec LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2025

Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2025

UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2025

BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 13, 2025

Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES…

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

Doehler North America, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 13, 2025

Favorite Day Bakery Frosted Sugar Cookies, 10 count, Net Wt 13.5 oz (383g). UPC - 85239-41250 3. Dist. By Target…

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

Give and Go Prepared Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 13, 2025

One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.

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

Intersurgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

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

Draeger, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1,…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700,…

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

Volcano Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and…

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…

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

Covidien

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2025

Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…

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

Mondelez Global LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2025

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2025

Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik…

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

World Market Management Services, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog…

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

Alcon Research LLC

2 more products 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.