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Use caution Medical device recall · FDA · Published August 22, 2019

ARJOHUNTLEIGH POLSKA Concerto & Basic Shower Trolly Recall: Risk of Patient Fall

ARJOHUNTLEIGH POLSKA recalls Concerto and Basic Shower Trolly models with potential safety catch failure that could cause patient falls. Affected units include specific model numbers and serial ranges. No remedy is stated in the recall notice.

🇺🇸 FDA recall #Z-1452-2020Medical deviceARJOHUNTLEIGH POLSKA ›
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Recalling firmARJOHUNTLEIGH POLSKA Sp. z.o.o.Ui. Ks. Piotra Wawrzyniaka 2 · Komorniki, Poland
✎ GovInfoNow plain-language explainer

ARJOHUNTLEIGH POLSKA is recalling Concerto and Basic Shower Trolly models due to a risk that safety catches might fail, potentially causing the trolley to open and leading to patient falls. This could result in injuries if a patient falls. Read more at govinfonow.com/recall/67110-arjohuntleigh-polska-concerto-basic-shower-trolly-recall-risk-of-patient.

Source Summary by GovInfoNow · govinfonow.com/recall/67110-arjohuntleigh-polska-concerto-basic-shower-trolly-recall-risk-of-patient · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1452-2020

Cite this page

“ARJOHUNTLEIGH POLSKA Concerto & Basic Shower Trolly Recall: Risk of Patient Fall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67110-arjohuntleigh-polska-concerto-basic-shower-trolly-recall-risk-of-patient. Based on FDA recall #Z-1452-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1452-2020%22&limit=1).

The FDA announced on 2019-08-22 that ARJOHUNTLEIGH POLSKA Sp. z.o.o. is recalling Concerto & Basic Shower Trollys due to a potential patient fall hazard. The firm initiated this voluntary Class II recall after discovering mechanical failures in the safety catches.

How to tell if you have it

  • Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102
  • Concerto & Basic Shower Trolly, Model Number BAB1007-01 (UDI: (01)05055982796255)
  • Concerto & Basic Shower Trolly, Model Number BAB1101-01 (UDI: (01)05055982787949)
  • Concerto & Basic Shower Trolly, Model Number BAB1102-01 (UDI: (01)05055982796156)
  • Concerto & Basic Shower Trolly, Model Number BAB1103-01 (UDI: (01)05055982796163)
  • Concerto & Basic Shower Trolly, Model Number BAB1107-01 (UDI: (01)05055982796187)
  • Concerto & Basic Shower Trolly, Model Number BAB2000-01 (UDI: (01)05055982788106)
  • Concerto & Basic Shower Trolly, Model Number BAB2101-01 (UDI: (01)05055982788007)
  • Concerto & Basic Shower Trolly, Model Number BAB2102-01 (UDI: (01)05055982796194)
  • Concerto & Basic Shower Trolly, Model Number BAB3000-01 (UDI: (01)05055982788120)
  • Concerto & Basic Shower Trolly, Model Number BAB3101-01 (UDI: (01)05055982788021)
  • Concerto & Basic Shower Trolly, Model Number BAB3107-01 (UDI: (01)05055982796248)
  • Concerto & Basic Shower Trolly, Model Number BAB5000-01 (UDI: (01)05055982788144)
  • Concert & Basic Shower trolleys Serial Numbers: P0512263 to P0551621, P0279164, SEE0643339, SEE0605124,P0249502, SEE045073, SEE0520032, 1106000338, SEE0348065, P0422951, P0232526
  • Concerto & Basic Shower Trolley Spare parts (safety catch) part no. 8451622, 8546608, S8533571-031, S8533572-031, S8533570-031 S8542201-014, S8523559-031

The hazard

The firm has become aware that any of the 4 safety catches may exhibit a mechanical failure, specifically a break in one of the arms of the safety catch. This failure 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.

Context

GovInfoNow's records show ARJOHUNTLEIGH POLSKA Sp. z.o.o. has 6 other recalls on record since 2018-10-22. Other recent recalls of similar products include Arjo Tenor Patient Lift Recall (2026-03-10), Arjo medical beds with IndiGo Drive wheels recall (2023-08-29), and Sara Plus Active Floor Lift Recall (2022-04-05). Other recent recalls of similar products include Olymp ShockPulse-SE Lithotripsy System Generator Recall (2025-11-14), Kiwi Omni Vacuum Delivery System Recall (2026-03-09), and Accuray Cyberknife System Recall (2026-06-16).

How to tell if you have this one

Check for model numbers BAB1000-01, BAB1000CON6102, and other listed models. Look for serial numbers between P0512263 and P0551621, as well as specific serial numbers like P0279164 and SEE0643339.

  • Brand
    ARJOHUNTLEIGH POLSKA
  • Product
    Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Model Numbers

    Identify if your shower trolley has model numbers BAB1000-01, BAB1000CON6102, or other listed models.

  2. Check Serial Numbers

    Look for serial numbers in the range P0512263 to P0551621 or specific serial numbers like P0279164 and SEE0643339.

Where it went and when

Where it was distributed

Distributed in 15 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “US: CA, CO, CT, GA, MA, MD, MI, NC, NJ, NY, OH, OK, TX, VA, WI OUS: Australia Austria, Bangladesh, Belgium, Canada, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, Iceland, India, Ireland, Italy, Japan, Korea, Luxembourg,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Colorado, Connecticut, Georgia, Maryland, Massachusetts, Michigan, New Jersey, New York, North Carolina, Ohio, Oklahoma, Texas, Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 2.5 years after the firm started it.

1. Firm started the recall: Aug 22, 201912. FDA classified it Class II: Mar 6, 202023. Published in FDA’s Enforcement Report: Mar 18, 202034. FDA terminated the recall: Feb 15, 2022420192022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1452-2020 (August 22, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1452-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA