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Showing 12821–12840 of 35905 results

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ROi CPS LLC: regard SPINE PACK , NU00193N, Item Number 880179014; neu...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard LATERAL SHOULDER, OR01044C, Item Number 880435003;...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard SHOULDER PK, GS00125U, Item Number 880120021; ort...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

Moderate

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard MINOR DAVINCI PACK, GS00349M, Item Number 88025101...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard HIP ARTHROSCOPY, OR01092B, Item Number 880462002; ...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard SHOULDER, GS00828G, Item Number 880367007; ortho s...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard DAVINCI PACK, GS00137W, Item Number 880132023; ga...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

ROi CPS LLC: regard SPINE, OR01100A, Item Number 880468001; ortho surg...

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDAOct 20, 2022FL, LA, MO +1 more• ROi CPS LLC

2023 VOLVO S90 Recall: ENGINE AND ENGINE COOLING:ENGINE:ENGINE CONTROL MODULE (ECU/ECM)

Volvo Car USA, LLC (Volvo Car) is recalling certain 2022-2023 S60, V60, S90L, XC60, and XC90 vehicles. An electronic control module (ECM) software error may prevent the combustion engine from starting, causing a loss of drive power.

NHTSAOct 20, 2022Nationwide• VOLVO

2022 KALMAR OTTAWA T2 Recall: ENGINE AND ENGINE COOLING:ENGINE:ENGINE CONTROL MODULE (ECU/ECM)

Kalmar Solutions, LLC (Kalmar) is recalling certain 2022 Ottawa T2 vehicles equipped with certain Cummins diesel engines. The engine control module (ECM) may experience an internal electrical short-circuit, causing the engine to stall.

NHTSAOct 19, 2022Nationwide• KALMAR

2023 SPARTAN K2 Recall: SERVICE BRAKES, AIR:SUPPLY:RESERVOIR/TANK

Shyft Group is recalling certain 2021-2023 Spartan K2 RV Chassis. The air brake supply reservoir is less than 12x the combined volume of air for all service brake chambers. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."

NHTSAOct 19, 2022Nationwide• SPARTAN

2023 THOR MOTOR COACH OMNI Recall: EQUIPMENT:OTHER:LABELS

Thor Motor Coach (TMC) is recalling certain 2023 Magnitude and Omni vehicles. The Occupant and Cargo Carrying Capacity (OCCC) Label states the incorrect number of seat belts, indicating that there are more seat belts available than there actually are. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other Than Passenger Cars."

NHTSAOct 19, 2022Nationwide• THOR MOTOR COACH

2022 EDGE TRAILERS NCH Recall: SUSPENSION:MULTIPLE AXLE

Innovative Specialties LLC (Innovative Specialties) is recalling certain 2022-2023 Nitro and Edge trailers. The rubber installed between the axle and trailer frame may deteriorate.

NHTSAOct 19, 2022Nationwide• EDGE TRAILERS

Bio-Rad Laboratories, Inc.: CMV IgM EIA, in vitro diagnostic.

Due to an unusual increase in the positivity rate with human IgM antibodies to cytomegalovirus (CMV) Enzyme Immunoassay (EIA).

FDAOct 19, 2022CA, CO, FL +11 more• Bio-Rad Laboratories, Inc.

BILT HELMET GROMMET BOLT YOUTH HELMET Equipment Recall: EQUIPMENT:MOTORCYCLE:HELMETS

Comoto Holdings, Inc. (Comoto) is recalling certain Bilt Grommet Youth and Grommet Bolt Youth helmets with part numbers BLH137 and BLH138; in sizes SY, MY, and LY. The helmet may not adequately protect the wearer in the event of a head impact during a crash. As such, these helmets fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 218, "Motorcycle Helmets."

NHTSAOct 18, 2022Nationwide• BILT HELMET

2023 KENWORTH T800B Recall: STEERING:LINKAGES:TIE ROD ASSEMBLY

PACCAR Incorporated (PACCAR) is recalling certain 2023 Peterbilt 348, 367, 389, 548, 567, and Kenworth T370, T480, T800, T800B, T880, W900B, and W990 vehicles. The tie rod clamps may have been improperly heat-treated, causing them to fail and allowing the tie rods to separate.

NHTSAOct 18, 2022Nationwide• KENWORTH

2021 HARLEY-DAVIDSON FLTRXS Recall: EXTERIOR LIGHTING:BRAKE LIGHTS

Harley-Davidson Motor Company (Harley-Davidson) is recalling certain 2019-2022 Trike and CVO Trike and 2020-2022 Touring and CVO Touring motorcycles. Please refer to Addendum A for specific vehicle model details. Due to a software error, the brake lights may illuminate without the rider applying the brakes. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

NHTSAOct 18, 2022Nationwide• HARLEY-DAVIDSON

Atrium Medical Corporation: Atrium Ocean Wet Suction Water Seal Chest Drain- Product ...

Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.

FDAOct 18, 2022Nationwide• Atrium Medical Corporation

Baxter Healthcare Corporation: Hill-Rom Progressa Bed System

The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.

FDAOct 18, 2022Nationwide• Baxter Healthcare Corporation

ARROW INTERNATIONAL Inc.: Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow Auto...

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

FDAOct 17, 2022Nationwide• ARROW INTERNATIONAL Inc.

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