Z-2055-2018 Class II Terminated
FDA device recall Z-2055-2018 was initiated by Becton Dickinson & Company on Feb 13, 2018 and is designated Class II. Reason for recall: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube The recall status is terminated (terminated Mar 9, 2020). Affected quantity: 9,568,900 total products.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 13, 2018
- Initiation Date
- Feb 13, 2018
- Termination Date
- Mar 9, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9,568,900 total products
Product Description
BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983
Reason for Recall
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube
Distribution Pattern
US Nationwide, Argentina, Belize , Brazil, Canada, China, Guam, India, Japan, Mexico, Nicaragua, Pakistan, Philippines, Singapore, Suriname, Taiwan
Code Information
1) UDI DI (01)50382903679831 PI (17)180531(10)7135828(30)1000 Lot/Serial # 7315828 Exp Date 5/31/2018 2) UDI DI (01)50382903679831 PI (17)180531(10)7146901(30)1000 Lot/Serial # 7125692 Exp Date 4/30/2018
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2055-2018
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026