Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Inventia Healthcare Private Limited

Inventia Healthcare Private Limited Recalls

All product recalls associated with Inventia Healthcare Private Limited.

Get alerts for this brand

Recall Summary

Total Recalls

451

Past Year

Class I (Serious)

Most Recent

Sep 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 321–340 of 451 recalls

Duloxetine Capsules 30mg (Inventia Healthcare) – Capsule Shell Defect (2016)

Failed Tablet/Capsule Specifications: Capsule shell (s) opening inside the bottle The Initial reports stated one or two capsules in a bottle count of 30s opening. First report came in June 14, 2016. Till date about 22 reports have come in from pharmacies which report two batches 130/16/001 and 130/16/002. Third batch 130/16/003 is not distributed yet, will be recalled from warehouse.

Class IIModerate

FDAOct 19, 2016Nationwide• Inventia Healthcare Private Limited

Residential Hydraulic Elevators (Cambridge Elevating) - Safety Hazard (2015)

This recall involves Elmira Hydraulic residential hydraulic elevators. The elevators were installed in homes with multiple floors. They have a manual accordion-style car gate door with vinyl laminate inserts and a control panel with up and down buttons, light switch, telephone, emergency stop button and power failure light. "Cambridge Elevating" is printed on the elevator's push button panel.

CPSCMar 19, 2015Nationwide• Cambridge Elevating, of Canada

1...15 161718 19...23

Page 17 of 23Next

Clinical Innovations, LLC: Ebb Complete Tamponade System, BD-OTS Obstetric Catheter,...

Potential for a balloon leak in all lots of (CTS-1000) manufactured since August 2014.

Class IIModerate

FDADec 30, 2014Nationwide• Clinical Innovations, LLC

DS-5500 Digital Audio Recorders (Olympus) – burn hazard (2014)

Fire/Burn Risk

This recall involves Olympus digital audio recorders with model number DS-5500. The recorders are black, measure about 4.5 inches tall by 1.9 inches wide by .67 inches thick. "Olympus" and "Digital Voice Recorder DS-5500" are printed on the front of the recorder. The recorder has three smart buttons, slide switches, edit functions, 2 GB of memory, an external SD card slot and a 1.7-inch LCD display on the front.

CPSCNov 19, 2014Nationwide• Olympus Imaging America Inc., of Center Valley, Pa.

Maquet Cardiovascular Us Sales, Llc: Maquet Quadrox-ID Pediatric Diffusion Membrane Oxygenator...

Maquet has confirmed through a customer complaint that while the oxygenators and the pouches for a single lot of Quadrox-ID Pediatric Diffusion Membrane Oxygenator with Bioliine Coating are labeled correctly with the Bioline coating, the individual cartons and 4-pack shipping containers of this lot incorrectly bear Softline coating labels instead of the bioline coating labels.

Class IIModerate

FDANov 5, 2014IN, MA, MI +1 more• Maquet Cardiovascular Us Sales, Llc

Maquet Cardiovascular Us Sales, Llc: Cardiohelp-I System Product Usage: A blood oxygenati...

Cardiohelp- i System may have a software issue that can potentially result in an erroneous display of a "Battery Needs Service" message after startup of the units when using either AC or DC power

Class IIModerate

FDAOct 17, 2014Nationwide• Maquet Cardiovascular Us Sales, Llc

Dark Chocolate Cherries (Tropical Valley) – Undeclared Peanuts (2014)

Undeclared Nuts

Next by Nature brand Dark Chocolate Cherries Lot 460013 may contain undeclared peanuts (from bulk product).

Class IIModerate

FDASep 26, 2014CA, CO, FL +8 more• Tropical Valley Foods, Inc.

Terumo Cardiovascular Systems Corporation: Hercules 360 Universal Stabilizing Arm, top mount, 360-de...

Terumo Cardiovascular Systems (Terumo CVS) is recalling certain lots of Hercules TM 360 Universal Stabilizing Arms because the two pins that hold the sleeve attached to the distal end of the device may come loose, causing the pins and sleeve to separate from the device. While the arm can still function without the pins and sleeve in place, there is potential for the loose components to fall into the surgical site.

Class IIModerate

FDAAug 20, 2014Nationwide• Terumo Cardiovascular Systems Corporation

Medtronic Cardiovascular Surgery-the Heart Valve Division: Hancock Apical Left Ventricle Connector, Model No. H174Ax...

Medtronic has decided to discontinue production and distribution of this low-volume product.

Class IIModerate

FDAAug 15, 2014IN, MD, TX• Medtronic Cardiovascular Surgery-the Heart Valve Division

Maquet Cardiovascular, LLC: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV...

Laceration Risk

An internal finding identified the presence of pinholes/cuts in some of the Tyvek pouches of the vacuum tubing sets included as an accessory to Acrobat V Vacuum Off-Pump System, Acrobat SUV Vacuum Off-Pump System, Axius XPOSE 3 Access Device and XPOSE 4 Access Device.

Class IIModerate

FDAAug 13, 2014Nationwide• Maquet Cardiovascular, LLC

Dark Chocolate Bananas (Tropical Valley) – undeclared allergens (2013)

Undeclared Allergen

The product contains the undeclared allergens walnuts and milk.

Class IHigh

FDAApr 12, 2013CO, MI, NJ +1 more• Tropical Valley Foods, Inc.

Wood Cleaner and Brightener (Cabot Stains) – Burn Risk (2012)

Fire/Burn Risk

Both products come in 1.3 gallon white handle tanks with black pump assembly and sprayer hose. The front has a yellow Cabot label with the product name. The back panel label contains instructions for use and product information and UPC codes 080351810503 on the Wood Cleaner bottles and 080351810497 on the Wood Brightener bottles.

CPSCSep 27, 2012Nationwide• Cabot Stains, a division of Valspar Corp., of Newburyport, Mass.

Evanix Air Rifles (Meca Evanix) – safety malfunction (2012)

Fire/Burn Risk

This recall involves Evanix Speed .177, .22 and .25 caliber rifles and Evanix Conquest .177, .22 and .25 caliber rifles. The rifle is a pre-charged pneumatic air rifle powered by a compressed air cylinder.

CPSCApr 18, 2012Nationwide• Meca Evanix of South Korea

Outdoor Playsets (Escalade Sports) – Fall Hazard (2011)

This recall involves belt-style swing seats on four models of Oasis Playsets: PG01W, PG02W, PG03W and PG04W. Model numbers are located on a plate on the swing's horizontal beam. The green plastic seats are about 26 inches long and are hung from green, plastic-coated chains. The swing seats have rounded ends with black grommets on each end. Printed on one side of the seat is: MADE IN CHINA GUARANTEED FOR ONE YEAR ADULT SUPERVISION REQUIRED DO NOT INSTALL IN AREAS WHERE TEMPERATURES EXCEED 120DEG F Printed on the other side of the seat is: WARNING IMPROPER USE MAINTENANCE INSTALLATION OR VANDALISM CAN DAMAGE SEAT AND LEAD TO SERIOUS INJURY FOR RESIDENTIAL USE BY ONE CHILD

CPSCFeb 8, 2011Nationwide• Escalade Sports of Evansville, Ind.

Maquet Cardiovascular, LLC: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System; Man...

During routine production quality monitoring process, it was found that UV curing adhesive was not used in a limited number of devices.

FDADec 17, 2009Nationwide• Maquet Cardiovascular, LLC

Maquet Cardiovascular, LLC: VASOVIEW 7xB Endoscopic Vessel Harvesting System; Manufac...

During routine production quality monitoring process, it was found that UV curing adhesive was not used in a limited number of devices.

FDADec 17, 2009Nationwide• Maquet Cardiovascular, LLC

Maquet Cardiovascular, LLC: VASOVIEW 6 Endoscopic Vessel Harvesting System Manufactur...

During routine production quality monitoring process, it was found that UV curing adhesive was not used in a limited number of devices.

FDADec 17, 2009Nationwide• Maquet Cardiovascular, LLC

LINA Medical ApS Formervangen 5 Glostrup Denmark: LiNA Loop Endoscopic Monopolar Loop for LSH (Laparoscopic...

Potential for the LiNA Loop to break during operating procedure.

FDADec 1, 2009GA, IN, MA +4 more• LINA Medical ApS Formervangen 5 Glostrup Denmark

Perfect Flame Gas Grills (Lucas Innovation) – Fire Risk (2009)

Fire/Burn Risk

The recalled grills are SLG series "Perfect Flame" brand outdoor propane or natural gas grills. The grills are stainless steel and painted black or gray metal. The model numbers affected by this recall are listed below. The model number can be found in the compartment under the cooking chamber. No other Perfect Flame model numbers are included in this recall. Model Replacement Burners Replacement Lid SLG2006B Yes No SLG2006BN Yes No SLG2006C Yes No SLG2006CN Yes No SLG2007A Yes Yes SLG2007B Yes Yes SLG2007BN Yes Yes SLG2007D Yes No SLG2007DN Yes No SLG2008A Yes Yes

CPSCNov 18, 2009Nationwide• Lucas Innovation Inc., of China

Terumo Cardiovascular Systems Corporation: Terumo Backplate Replacement CXFVR 1500 Holder The Flexi...

Backplate reservoir holders were manufactured with an incorrect configuration of connector supports. The devices were manufactured and configured with two 3/8 inch and one inch connector supports instead of one 3/8 inch and two inch connector supports (See location of supports as # 7 and # 8 on backplate attachment). The backplates were manufactured as described in manufacturing instructions a

FDAOct 2, 2009Nationwide• Terumo Cardiovascular Systems Corporation