Med-Mizer, Inc. recalls Sit to Stand STS500 Patient Lift
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.
Read the official notice →- Date
- 2023-03-08
- Country
- United States
- Brand
- Med-Mizer, Inc.
- Product
- Sit to Stand STS500 Patient Lift
- Classification
- Class II
- Units
- Awaiting consignee list from the recalling firm.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
Other drugs & medical recalls in the United States
- 2023-03-09
USSandoz Recalls Aprepitant Capsules and Lidocaine and Prilocaine Cream Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
The recalled prescription drugs and products that contain lidocaine must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant,…
- 2023-03-08
- US
Coltene Whaledent Inc recalls SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of carious material, reducing hard tooth structure, cavity preparation,…
Screw connection between the turbine head and the push button may loosen and fall off during the treatment, and increase the risk of swallowing or inhaling part of the turbines head or the push button
FDA · DeviceColtene Whaledent IncNationwide Foreign: Canada Germany Indonesia Ireland Lebanon Saudia Arabia…Official notice → - US
Carestream Health, Inc. recalls DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality radiographic images to…
After pressing and releasing the Z-Axis Motorized buttons on the Tube Head Display, the Overhead Tube Crane (OTC) could potentially continue the movement unexpectedly to a certain distance which could potentially…
FDA · DeviceCarestream Health, Inc.Worldwide distribution - US Nationwide distribution in the states of…Official notice → - US
SEDECAL SA recalls Phoenix mKDR Xpress, digital mobile diagnostic x-ray system
Sedecal was informed of 3 incidents of erratic movements related to X-ray mobile systems.
- US
Biomerieux Inc recalls MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects microbiology laboratory instruments for ID/AST and…
For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as part of their workflow, AST filter rules that have been activated are not always being applied to AST results when sending the results to the…
FDA · DeviceBiomerieux IncUS Nationwide distribution to the states of Alabama, California, North…Official notice → - US
Beaver Visitec International, Inc. recalls Ultracell Wick with 80cc Collection Bag, 20/box
Device packaging may contain open seals, compromising product sterility.
FDA · DeviceBeaver Visitec International, Inc.US distribution in AL, CA, CO, DC, FL, GA, IL, LA, MD, MN, MT, NC, NH, NJ, NM,…Official notice →