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Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill.

Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill. Recalls

All product recalls associated with Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill..

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

Most Recent

Jan 2026

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 2261–2280 of 7756 recalls

Bella Residential Elevators (Bella) – child entrapment (2022)

This recall involves Bella residential elevators manufactured from 2009 to 2021. Models include Symmetry IGD, Hydraulic, and Winding Drum Elevators. The Symmetry brand name is located on the elevators' controllers. The elevators are used in consumers' homes.

CPSCJan 11, 2022Nationwide• Bella Elevator, LLC, d/b/a Symmetry Elevating Solutions, of Peoria, Ill.

BASE 10 GENETICS INC: RNAstill Molecular Transport Medium Vial, Catalog number ...

The product does not have 510(k) clearance.

FDAJan 10, 2022Nationwide• BASE 10 GENETICS INC

Compass Health Brands (Corporate Office): Voyager Rollator-intended as a mechanical walker Model Nu...

Laceration Risk

Wheel spoke may crack causing the wheel to separate from the axle may result in patient injuries, including bruising and lacerations requiring stitches.

1...112 113114115 116...388

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FDAJan 10, 2022Nationwide• Compass Health Brands (Corporate Office)

Mucus Relief D (Dr. Reddy's) – Subpotent Drug (2022)

Subpotent drug

Class IIILow

FDAJan 10, 2022Nationwide• Dr. Reddy's Laboratories, Inc.

Acon Biotech (Hangzhou) Co., Ltd.: Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing), CE...

Non-EUA authorized, CE marked, SARS-CoV-2 antigen rapid test kits are being recalled from the U.S. market because use may lead to inaccurate test results, including false negative or false positive test results.

FDAJan 9, 2022MD, PA• Acon Biotech (Hangzhou) Co., Ltd.

Baxter Healthcare Corporation: Baxter Equipo de transferencia para DP MiniCap de vida ut...

Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.

FDAJan 7, 2022Nationwide• Baxter Healthcare Corporation

Orthosoft, Inc. dba Zimmer CAS 3300-75 Queen St Montreal Canada: NavitrackER Kit A: Knee, Model Number 20-8000-000-07,

The product was released for distribution without passing sterilization results, which could potentially lead to insufficient sterility of the product. The highest severity risk is infection leading to surgical intervention.

FDAJan 7, 2022Nationwide• Orthosoft, Inc. dba Zimmer CAS 3300-75 Queen St Montreal Canada

Baxter Healthcare Corporation: Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Se...

FDAJan 7, 2022Nationwide• Baxter Healthcare Corporation

Baxter Healthcare Corporation: Baxter MiniCap Extended Life PD Transfer Set (Easy-Lock),...

FDAJan 7, 2022Nationwide• Baxter Healthcare Corporation

BALT USA, LLC: The Optima Coil System consists of an implantable emboliz...

Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf carton label or pouch label due to inadequate manufacturing line clearance. As a result of this labeling mix-up, there is the possibility of inadvertently selecting the incorrect coil size for the procedure potentially causing some harms like vessel damage, an inability to treat with said device and potential rupture of the aneurysm.

FDAJan 4, 2022Nationwide• BALT USA, LLC