Hill-Rom, Inc. recalls (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko…
Traverse rail carriage delivered with non-conforming screws are too short to ensure appropriate installation. There is potential that the screws are unable to secure the traverse rail appropriately and could loosen…
Read the official notice →- Date
- 2022-03-23
- Country
- United States
- Brand
- Hill-Rom
- Product
- (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of AT, CA, CZ, DE,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
More Hill-Rom recalls
- 2022-02-23
USHill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
FDA · DeviceHill-Rom, Inc.Worldwide distribution - US Nationwide and the countries of Austria, Austria,…Official notice →- 2021-12-29
- US
Hill-Rom Inc. recalls These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call, Part Number 4.0…
An unrecoverable error may occur where a component will fail to complete the reboot cycle, become non-functional and must be replaced.
- 2021-10-06
- US
Hill-Rom, Inc. recalls LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC, Wide Model Number: 3156065B (obsolete since 12JUN2020) - The…
Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may…
FDA · DeviceHill-Rom, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
Other drugs & medical recalls in the United States
- 2022-03-23
- US
LivaNova Deutschland GmbH recalls Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System…
One ferrite ring expected to be installed on centrifugal pump system power cable may not be present.
- US
Wright Medical Technology, Inc. recalls Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC…
An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
FDA · DeviceWright Medical Technology, Inc.International distribution to the country of France.Official notice → - US
Microbiologics Inc recalls Mycoplasma genitalium Control Panel (Inactivated Pellet)
Distributed product did not undergo proper release testing.
FDA · DeviceMicrobiologics IncDistribution in US: AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY,…Official notice → - US
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls LINQ II Insertable Cardiac Monitor
Devices may lose functionality due to susceptibility to moisture ingress.
FDA · DeviceMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)Worldwide distribution - US Nationwide distribution in the states of NJ, NY,…Official notice → - US
Boston Scientific Corporation recalls HYDRATOME RX 44-20MM/450CM Material Number: M00583060
Sterility of device is compromised due to a sterile barrier breach
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
Hologic, Inc recalls Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X Fusion Capture…
Failed stability specifications for reagent kits that may result in false negative test results.
FDA · DeviceHologic, IncWorldwide distribution - US Nationwide distribution in the states of AR, CA,…Official notice →