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H:20 Innovations LLC

H:20 Innovations LLC Recalls

All product recalls associated with H:20 Innovations LLC.

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Recall Summary

Total Recalls

266

Past Year

Class I (Serious)

Most Recent

Nov 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 241–260 of 266 recalls

Pediatric Electrolyte (H:20 Innovations) – seal defect (2014)

H:20 Innovations is recalling Meijer Brand Baby Pediatric Electrolyte Fruit and Strawberry Flavor 8oz drinks due to a seal defect found during a complaint investigation.

Class IIModerate

FDAMar 26, 2014MI, OH• H:20 Innovations LLC

Terrain Zyme Myco-Zyme (Innovative Labs) – Antimicrobial Agent Detected (2013)

Innovative Labs, LLC. has recalled two Dietary Supplements due to the presence of Chloramphenicol, an antimicrobial agent.

Class IIModerate

FDAOct 14, 2013CA• Innovative Labs, LLC

Terrain Zyme LGS-Zyme (Innovative Labs) – Antimicrobial Agent Detected (2013)

Innovative Labs, LLC. has recalled two Dietary Supplements due to the presence of Chloramphenicol, an antimicrobial agent.

Class II

1...11 121314

Page 13 of 14Next

Moderate

FDAOct 14, 2013CA• Innovative Labs, LLC

Light & Fit Yogurt (Dannon) – Metal Fragment Risk (2012)

The recalled products may potentially contain metal fragment(s) from a faulty manufacturing part.

Class IIModerate

FDAOct 23, 2012Nationwide• The Dannon Company, Inc - Discovery & Innovation Center

Activia Light Yogurt (Dannon) – Metal Fragment Risk (2012)

The recalled products may potentially contain metal fragment(s) from a faulty manufacturing part.

Class IIModerate

FDAOct 23, 2012Nationwide• The Dannon Company, Inc - Discovery & Innovation Center

Prestigio Office Chair (True Innovations) – Fall Risk (2012)

This recall involves Prestigio model leather office chairs. The high-back leather chairs were sold in black and have a five-leg metallic finish base with casters. The SKU number 181-265 and the words "Realspace Soho" and "Prestigio High-Back Chair Black Leather" are printed on a label located on the underside of the seat.

CPSCSep 13, 2012Nationwide• True Innovations LLC, of Hong Kong, China

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

Data Innovations, Inc.: Instrument Manager -Software Versions 8.05, 8.06, 8.07, 8...

The "previous result" retrieved from the Specimen Management Database may not be the most recent "previous result".

FDAMay 11, 2009Nationwide• Data Innovations, Inc.

Innovative Implant Technology: Sinu-Lift(TM) System, LLC., Model SLS-1, Sterile, Innovat...

Laceration Risk

Possible device failure: The cutter's shaft of the Sinu-Drill of the Sinu-Lift System could potentially get stuck inside the tap, thereby not allowing the cutter to spring out of the tap upon encountering the sinus membrane, increasing the possibility of perforating the sinus membrane.

FDASep 30, 2008Nationwide• Innovative Implant Technology

Gas Grill (Perfect Flame) - Fire Hazard (2008)

Fire/Burn Risk

This recall involves Perfect Flame brand grills, Model GAC3615 four-burner LP gas grills. The grill has two lids. "Perfect Flame" is printed on the larger lid. The model number, serial number, and date code are printed on a label on the right side cart frame panel. The following serial numbers and date codes are included in this recall. Model Number Date Code Serial Number GAC3615 KU (July 07) 000001 - 001278 001282 - 001423 KV (Aug. 07) 001424 - 001849 001855 - 005404 KW (Sept. 07) 005405 - 006540 006548 - 009671 010299 - 010440 KX (Oct. 07) 010005 - 010297 010441 - 014305 014322 - 017164 KY (Nov. 07) 017165 - 020714 020715 - 022856 KZ (Dec. 07) 022859 - 023284 024301 - 025862

CPSCAug 7, 2008Nationwide• Lucas Innovation Inc., of China

Innovative Neurotronics, Inc.: WalkAide Stimulator System Control Module, Part Number 20...

Knob responsible for regulating the amount of stimulation administered by the WalkAide System control unit may fall off while device is in use.

FDAAug 6, 2008Nationwide• Innovative Neurotronics, Inc.

Clinical Innovations, LLC: ClearView Uterine Manipulator, Long tip version with disp...

Inadequate package seal could compromise sterility.

FDAMay 12, 2008CA, CO, FL +3 more• Clinical Innovations, LLC

Innovacon Inc: Fisher Healthcare Sure-Vue Serum/Urine hCG-STAT; in vitro...

Laceration Risk

Incorrect results: The Sure-Vue Serum/Urine hCG-STAT test, when interpreted at extended read times, may exhibit sensitivity to patient samples containing hCG at levels well below the cut-off, potentially resulting in a false positive interpretation by the user.

FDAOct 1, 2007Nationwide• Innovacon Inc

AMS Innovative Center San Jose: American Medical Systems, Inc., (AMS) GreenLight HPS Fibe...

Control knob break: The knob used to finely control the direction of the laser energy may break.

FDAJun 18, 2007Nationwide• AMS Innovative Center San Jose

AMS Innovative Center San Jose: GreenLight HPS System, Surgical Laser System and Accessor...

Component missing: Some products were issued without thermal protection switches.

FDAApr 17, 2007Nationwide• AMS Innovative Center San Jose

Data Innovations, Inc.: Roche Cobas driver (rchcob6i), analytical laboratory data...

Software of modular driver may incorrectly report patient results as Quality Control Results

FDANov 3, 2006Nationwide• Data Innovations, Inc.

Data Innovations, Inc.: Roche Modular Drive (rchmdlri), analytical laboratory dat...

Software of modular driver may incorrectly report patient results as Quality Control Results

FDANov 3, 2006Nationwide• Data Innovations, Inc.

Data Innovations, Inc.: Data Innovations Instrument Manager Version 8:00, 8.01, 8...

Patient results may be associated with an incorrect specimen

FDAAug 10, 2006Nationwide• Data Innovations, Inc.

EM Innovations Inc: Model EMI 82691, Stic Kit Needle Containment Device. The...

The firm failed to include User Instructions with the Stic Kit Needle Containment Device, Model EMI 82691, which they shipped to distributor/customers.

FDAApr 3, 2006IN, MO, NJ +3 more• EM Innovations Inc

In-Wall Volume Controls (Dana Innovations) – installation risk (2005)

Fire/Burn Risk

Sold under the brand names Architectural Audio and HomeTech, these in-wall volume controls were professionally installed as part of whole house audio systems. The switch plate covers for the recalled systems are white or almond, and "aVc" (amplified volume control) is imprinted above the volume control. They have the following model numbers: Brand Model Numbers Architectural Audio 20127 20128 HomeTech 10114 10115 The model number is not visible to the consumer, and consumers are instructed not to remove the keypads from the wall to look for a model number. All serial numbers are included in the recall.

CPSCOct 20, 2005Nationwide• Dana Innovations, of San Clemente, Calif.