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Recalls distributed in Indiana

These notices name Indiana 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.

4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Food

Reported Apr 29, 2020

Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE…

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

Champlain Chocolate Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 29, 2020

Siemens N Latex CDT Kit- IVD quantitative determination of carbohydrate-deficient transferrin (CDT) in human serum.…

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

CSL Behring GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

TCM4 Base unit, Ref 391-880, UDI:(01)05700693918808, used with the monitor modules TCM4 (902-778), TCM40 (902-778,…

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

Radiometer Medical ApS

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and Model RSPOl)…

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

Rayner Intraocular Lenses Limited

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901

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

Smith & Nephew, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model…

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

Abbott

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

Nitinol Thermocouple Electrode, 10 cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of…

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

Boston Scientific Neuromodulation Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin for Gases and Electrolytes

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

Smiths Medical ASD, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated…

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

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

"HEMOGLOBIN A1c CALIBRATORS *** REF 4P52-01 *** 307261/R03 *** S4P5X0 *** FOR USE WITH ARCHITECT" - Product Usage: use…

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended to be used in the anastomosis of veins and…

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

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.

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

Biomet, Inc.

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable…

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

James Leckey Design Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Lindt & Sprungli (USA), Inc.; Excellence 85% Cocoa Dark Chocolate; Net WT 3.5OZ (100g)

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

Lindt & Sprungli (USA), Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2020

ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

PRIVATE SELECTION FROZEN BERRY MEDLEY in 16 oz. (10 bags per case) and 48 oz. bags (6 bags per case). UPC: 0001111079120

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2020

Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2020

BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2020

Meijer Mixed Nuts with Peanuts & Sea Salt 16 Oz UPC: 7-19283-80863-9

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

Meijer Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2020

Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.

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

Merits Holdings Co. dba Merits Health Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Philips V60 Ventilators with Power Management PCBA part number 1055906

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

Respironics California, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…

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

Trilliant Surgical, LLC

10 more products in this recall

FDA (openFDA device enforcement)

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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.