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Trumpf Medical Systems, Inc.

Trumpf Medical Systems, Inc. Recalls

All product recalls associated with Trumpf Medical Systems, Inc..

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Recall Summary

Total Recalls

1000

Past Year

888

Class I (Serious)

124

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 12321–12340 of 17593 recalls

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

POWEREASE Instrument (Medtronic) – Retaining Tabs Issue (2014)

The retaining tabs component of the Set Screw Retaining Drive may be oversized, which will not allow proper mating between the Set Screw Retaining Drive and the set screw.

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Class II

Moderate

FDADec 3, 2014AR, CA, FL +13 more• Medtronic Sofamor Danek USA Inc

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

JUPITER Remote Control (Trumpf) – Unintended Movement (2014)

Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Class IIModerate

FDADec 3, 2014AL, AZ, CA +22 more• Trumpf Medical Systems, Inc.

Electrical Meter Breakers (Eaton) – Shock Hazard (2014)

This recall involves MBED 3042 series residential meter breaker. The meter breakers are service entrance equipment systems that consist of a single meter socket and load center or a meter socket and main breaker combined in one enclosure. The meter breakers have gray metallic enclosures and measure about 14 ¼ inches wide by 42 ½ inches high by 7 inches deep. The recalled units have catalog numbers MBED3042B200BF, MBED3042B200BF6, MBED3042B225PV or MBED3042PV200BF. The catalog number is located on the unit's packaging. The enclosures have a single warning label on the bottom of the lower right compartment door, which is secured with a latch and hasp at the bottom. Consumers should not open the meter breaker's enclosure.

CPSCDec 2, 2014Nationwide• Eaton Corporation, of Moon Township, Pa.

NexGen Knee Solution (Zimmer) – Fitting Problem (2014)

During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.

Class IIModerate

FDADec 2, 2014Nationwide• Zimmer Trabecular Metal Technology, Inc.

Raw Shelled Peanuts (Pea River) – Aflatoxin Contamination (2014)

Product testing at the supplier found aflatoxin above 20 ppb

Class IIModerate

FDADec 1, 2014AL• Pea River Peanut Company, LLC

SoftPath Laboratory Information System (SCC Soft Computer) – Diagnostic Text Issue (2014)

Modifications to diagnostic text may be: 1) Saved to the database but not appear on the report sent to the physician; or 2) Documented on the report, but not saved to the database.

Class IIModerate

FDANov 26, 2014Nationwide• SCC Soft Computer

VisiPlugST (Lacrimedics) – Moisture Breakdown Risk (2014)

Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart, or crumble upon contact. The firm's data also suggests that a 4 year shelf life may not be sustained.

Class IIILow

FDANov 26, 2014Nationwide• Lacrimedics Inc

Utility Vehicle Doors (Pro Armor) – Impact Risk (2014)

Laceration Risk

This recall involves Pro Armor doors sold as accessories for model year 2010 through 2014 Polaris RZR 800 and RZR 900 models. The doors have a black powder coated finish and have four major components: a large square sheet metal panel, a smaller triangular sheet metal panel, a tubular metal frame and a latch. The panels are interchangeable and come in two styles. One style has cutout vents along the top and the other style has none. The smaller panel has a white Pro Armor logo below the cutouts. The door frame has the logo and "Pro Armor" on the top tube. The latch is silver with a black locking mechanism that attaches to the vehicle frame and a handle that attaches to the door.

CPSCNov 25, 2014Nationwide• LSI Products Inc. dba Pro Armor, Riverside, Calif.

DRX-Revolution Mobile X-Ray System (Carestream) – Broken Bolt (2014)

While servicing a unit at a customer site, a field engineer discovered a broken bolt from the carriage assembly. Carestream has identified an issue related to the DRX-Revolution Mobile X-Ray System in which bolts that secure the x-ray tube assembly/boom to the device mounting block may break. It has been determined that this issue is a result of an improperly assembled part which holds the x-ray

Class IIModerate

FDANov 25, 2014Nationwide• Carestream Health Inc

Dasani Purified Water (Coca Cola Bottling) – potential mold (2014)

An equipment malfunction during production that may have led to the appearance of mold in some product.

Class IIILow

FDANov 24, 2014AL, FL, GA +1 more• Coca Cola Bottling Company United, LLC

Champion Defender (Champion) – Seat Defect (2014)

Champion Bus, Inc. (Champion) is recalling certain model year 2014-2015 LF Transport, HCAC, Defender, Crusader, and Challenger transit buses manufactured September 2, 2014, to October 14, 2014. The spring nuts used to secure the passenger seats failed durability testing.

NHTSANov 24, 2014Nationwide• CHAMPION

Aztec Cheddar Cheese (Flat Creek Farm) – Salmonella Contamination (2014)

Salmonella

Product was found to be contaminated with Salmonella.

Class IHigh

FDANov 24, 2014GA• Flat Creek Farm & Dairy

Low Country Gouda (Flat Creek Farm) – Salmonella Contamination (2014)

Salmonella

Product was found to be contaminated with Salmonella.

Class IHigh

FDANov 24, 2014GA• Flat Creek Farm & Dairy

Simplex 4100ES Fire Alarm Panel (Tyco) – activation failure (2014)

Fire/Burn Risk

The recalled Simplex 4100ES Fire Control Panel is an addressable fire alarm control panel that can support up to 2,500 addressable points, fire alarm and emergency voice communications and peer-to-peer networking operations. The metal cabinets containing the panel are red or white and measure about 22 inches to 56 inches in height, 24 inches in width and 7 inches in depth. The panels have Simplex 4100ES printed on the front of the panel.

CPSCNov 20, 2014Nationwide• Tyco International de Mexico, S. de R.L. de C.V.