ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 [(01)05056097364483], BAB1007-01 [(01)05055982796255], BAB1101-01 [(01)05055982787949], BAB1102-01 [(01)05055982796156], BAB1103-01 [UDI: (01)05055982796163], BAB1107-01 [(01)05055982796187], BAB2000-01 [UDI: (01)05055982788106], BAB2101-01 [(01)05055982788007], BAB2102-01 [01)05055982796194], BAB3000-01 [(01)05055982788120], BAB3101-01 [(01)05055982788021], BAB3107-01[ (01)05055982796248], BAB500 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 [(01)05056097364483], BAB1007-01 [(01)05055982796255], BAB1101-01 [(01)05055982787949], BAB1102-01 [(01)05055982796156], BAB1103-01 [UDI: (01)05055982796163], BAB1107-01 [(01)05055982796187], BAB2000-01 [UDI: (01)05055982788106], BAB2101-01 [(01)05055982788007], BAB2102-01 [01)05055982796194], BAB3000-01 [(01)05055982788120], BAB3101-01 [(01)05055982788021], BAB3107-01[ (01)05055982796248], BAB500
Brand
ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland
Lot Codes / Batch Numbers
Concert & Basic Shower trolleys Serial Numbers: P0512263 to P0551621, P0279164, SEE0643339, SEE0605124, P0249502, SEE045073, SEE0520032, 1106000338, SEE0348065, P0422951, P0232526
Products Sold
Concert & Basic Shower trolleys Serial Numbers: P0512263 to P0551621, P0279164, SEE0643339, SEE0605124,P0249502, SEE045073, SEE0520032, 1106000338, SEE0348065, P0422951, P0232526
ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland is recalling Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 due to The firm has become aware that any of the 4 safety catches may exhibit a mechanical failure (break in one of the arms of safety catch), which in certa. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm has become aware that any of the 4 safety catches may exhibit a mechanical failure (break in one of the arms of safety catch), which in certain circumstances may contribute to the side support unintentionally opening and may lead to a potential risk of a patient fall. The patient falling could lead to various types of injuries.
Recommended Action
Per FDA guidance
On 08/22/2019 a "Urgent - Field Safety Notice Medical Device correction" letter was sent to all affected consignees for the Concerto & Basic Shower Trolley. The notification informed consignees about the recall and asked they take the following action: 1. Verify the condition of all 4 Safety Catches attached to your device. If you notice the break withdraw the trolley from use. 2. IMPORTANT: The device may stay in use until the upgrade is performed, providing that the following instructions are carefully followed: - It is recommended that the Safety Catches on the shower trolley Side Supports be inspected daily to ensure any of the catches are not broken as show on the Image - The patient is not left unattended at any time. - The patient is fully assisted so that he/she does not grab, push or lean against the Side Supports during showering activities. - Caregivers should limit pulling and pushing of the Side Supports with excessive force. - Note: always adhere to the Safe Working Load as outlined in the IFU. 3. Ensure that all caregivers and users of Arjo Concerto & Basic shower trolleys are made aware of this Field Safety Notice (FSN) and all listed devices at your facility are available to be retrofitted free of charge during the service technician visit. 4. If you have purchased spare parts listed, any of the following will be done free of charge: a. If the spare parts were sold to a 3rd party, please provide the sold to information on the Customer Response Form. Arjo will contact the 3rd party to make arrangements for repair or return of the affected parts. b. If the purchased parts were installed on a Concerto/Basic unit in your inventory, please provide the serial number on the Customer Response Form so an Arjo technician can inspect and retrofit the unit. c. If the purchased parts are still in your inventory, please complete and return the Customer Response Form and Arjo will contact you and make arrangements to replace the spare
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CO, CT, GA, MD, MA, MI, NJ, NY, NC, OH, OK, TX, VA, WI
Page updated: Jan 10, 2026