Med-Mizer, Inc.: Med-Riser MR600 Patient Lift

Recall number

Z-1204-2023

Recalling firm

Med-Mizer, Inc.

Product

Med-Riser MR600 Patient Lift

Status

Open, Classified

Initiated

2023-02-03

Posted

2023-03-02

Terminated

not on file

Reason

Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.

Root cause

Device Design

Action

Med-Mizer notified distributors of this recall event by distributing an Urgent Medical Device Recall Notice on 02/03/2022 via Certified Mail. The MR600 and STS500 Patient Lifts are being subject to recall due to the potential for the nut securing the boom to become loose over time, which could result in the boom moving unexpectedly side to side or dropping the patient during operation. Customers are asked to inspect all affected devices at their facility to determine if the nut securing the boom is loose. If it is, immediately remove the device from service. Med-Mizer is providing customers with affected devices replacement parts in order to complete the correction. Customers are to complete the provided Correction Response Form to Med-Mizer and return via fax at (812)932-5678, by email at support@med-mizer.com, or by mail at 80 Commerce Drive, Batesville, IN 47006. If your firm is a distributor, please provide this notice to your customers. Any questions can be directed to Med-Mizer by phone at (877)867-7365.

Quantity

241 units

Distribution

Awaiting consignee list from the recalling firm.

Lot, serial or model codes

UDI-DI: 00852195007308; Serial No.: MR600000, MR600001, MR600002, MR600003, MR600004, MR600005, MR600006, MR600007, MR600008, MR600009, MR600010, MR600011, MR600012, MR600013, MR600014, MR600015, MR600016, MR600017, MR600018, MR600019, MR600020, MR600021, MR600022, MR600023, MR600024, MR600025, MR600026, MR600027, MR600028, MR600029, MR600030, MR600031, MR600032, MR600033, MR600034, MR600035, MR600036, MR600037, MR600038, MR600039, MR600040, MR600041, MR600042, MR600043, MR600044, MR600045, MR600046, MR600047, MR600048, MR600049, MR600050, MR600051, MR600052, MR600053, MR600054, MR600055, MR600056, MR600057, MR600058, MR600059, MR600060, MR600061, MR600062, MR600063, MR600064, MR600065, MR600066, MR600067, MR600068, MR600069, MR600070, MR600071, MR600072, MR600073, MR600074, MR600075, MR600076, MR600077, MR600078, MR600079, MR600080, MR600081, MR600082, MR600083, MR600084, MR600085, MR600086, MR600087, MR600088, MR600089, MR600090, MR600091, MR600092, MR600093, MR600094, MR600095, MR600096, MR600097, MR600098, MR600099, MR600100, MR600101, MR600102, MR600103, MR600104, MR600105, MR600106, MR600107, MR600108, MR600109, MR600110, MR600111, MR600112, MR600113, MR600114, MR600115, MR600116, MR600117, MR600118, MR600119, MR600120, MR600121, MR600122, MR600123, MR600124, MR600125, MR600126, MR600127, MR600128, MR600129, MR600130, MR600131, MR600132, MR600133, MR600134, MR600135, MR600136, MR600137, MR600138, MR600139, MR600140, MR600141, MR600142, MR600143, MR600144, MR600145, MR600146, MR600147, MR600148, MR600149, MR600150, MR600151, MR600152, MR600153, MR600154, MR600155, MR600156, MR600157, MR600158, MR600159, MR600160, MR600161, MR600162, MR600163, MR600164, MR600165, MR600166, MR600167, MR600168, MR600169, MR600170, MR600171, MR600172, MR600173, MR600174, MR600175, MR600176, MR600177, MR600178, MR600179, MR600180, MR600181, MR600182, MR600183, MR600184, MR600185, MR600186, MR600187, MR600188, MR600189, MR600190, MR600191, MR600192, MR600193, MR600194, MR600195, MR600196, MR600197, MR600198, MR600199, MR600200, MR600201, MR600202, MR600203, MR600204, MR600205, MR600206, MR600207, MR600208, MR600209, MR600210, MR600211, MR600212, MR600213, MR600214, MR600215, MR600216, MR600217, MR600218, MR600219, MR600220, MR600221, MR600222, MR600223, MR600224, MR600225, MR600226, MR600227, MR600228, MR600229, MR600230, MR600231, MR600232, MR600233, MR600234, MR600235, MR600236, MR600237, MR600238, MR600239, and MR600240.

510(k) numbers

not on file

PMA numbers

not on file

Product code

FSA

Firm FEI

3004976058

Firm city

Batesville

Firm state

IN

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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