CLASS II Device recall · Reported 8 Jun 2022 · FDA Enforcement Report
Cervical Tray recalled by Busse Hospital Disposables
Busse Hospital Disposables is recalling Cervical Tray, distributed nationwide in the US. The recall was initiated on 22 Feb 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1168-2022
- FDA event ID
- 90072
- Recalling firm
- Busse Hospital Disposables, Hauppauge, NY
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 22 Feb 2022
- FDA classified
- 28 May 2022
- Reported
- 8 Jun 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 22 Feb 2022 | Recall initiated by company | |
| 28 May 2022 | Classified by FDA | +95 days |
| 8 Jun 2022 | Published in enforcement report | +11 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products
Product as listed by the FDA
Cervical Tray Catalog Number: 3765R2
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products
Which lots are affected?
Lot Numbers: 2031213S 2130221S UDI: 00849233015203
Where was it sold?
Nationwide
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
57 other products · FDA event 90072This product is part of a recall event; the main page for the event is Pellet Insertion Tray recalled by Busse Hospital Disposables.
More recalls from Busse Hospital Disposables
All 63| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Catalog No. 800 Tracheostomy Care Tray - Sterile -Latex Free recalled | Busse Hospital Disposables | Sterility | Nationwide |
| Device | CLASS I | Catalog No. 1443 Dressing Change Tray / Sterile - Latex Free recalled | Busse Hospital Disposables | Sterility | Nationwide |
| Device | CLASS I | Catalog No. 9251R1, 9251R2, 9251R3 Tracheostomy Care SET / Sterile recalled | Busse Hospital Disposables | Sterility | Nationwide |
| Device | CLASS II | Busse Spine Injection Tray-Intended as a nerve block recalled | Busse Hospital Disposables | Other | TX |
| Device | CLASS II | Busse Joint Injection Tray -Intended as a nerve block recalled | Busse Hospital Disposables | Other | TX |
Other Other Medical Devices recalls
All 13,778| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Citric Complete Dry Citric Acid Concentrate recalled | Nipro Renal Soultions USA | Other | Nationwide |
| Device | CLASS I | Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | Halyard IV Start Kit Non-Sterile recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS I | Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | AMS Convenience Kit: Dsaek Pack - RX recalled | Windstone Medical Packaging | Device Malfunction | Nationwide |