Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Device

Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.

Agency Publication Date: February 7, 2018
Share:
Sign in to monitor this recall

Affected Products

Product: Safety-Deluxe Lumbar Puncture Tray, Catalog # 974 Product Usage: Surgical procedure

Lot Number/Expiration Date: 1) 1610300/Expiration Date 03/01/2019; 2) 1610503/Expiration Date 05/30/2019; 3) 1710059/Expiration Date: 09/30/2019; 4) 1610383/Expiration Date: 02/28/2019; 5) 1610463/Expiration Date: 05/30/2019; 6) 1610215/Expiration Date: 02/01/2019; 7) 1610114/Expiration Date: 11/01/2018; 8) 1610044/Expiration Date: 06/01/2018;

Lot Numbers:
Number
Product: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle, Catalog # 977 Product Usage: Surgical procedure

Lot Numbers/Expiration Dates: 1) 1610197/Expiration Date: 12/01/2018; 2) 1610277/Expiration Date: 03/01/2019

Lot Numbers:
Numbers
Product: Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure

Lot Numbers/Expiration Dates: 1) 1610197/Expiration Date: 12/01/2018; 2) 1610204/Expiration Date: 02/01/2019; 3) 1610075/Expiration Date: 06/01/2018; 4) 1610431/Expiration Date: 05/30/2019; 5) 1610246/Expiration Date: 02/01/2019; 6) 1610204/Expiration Date: 02/01/2019

Lot Numbers:
Numbers
Product: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle and Aspiration Needle Sterile, Catalog # 985 Product Usage: Surgical procedure

Lot Numbers/Expiration Dates: 1) 1720047/Expiration Date: 02/20/2018

Lot Numbers:
Numbers
Product: Laceration Tray, Catalog # 1892R1 Product Usage: Surgical procedure

Lot Numbers/Expiration Dates: 1) 1730650/Expiration Date: 10/30/2021; 2) 1630921/Expiration Date: 11/02/2020; 3) 1631124/Expiration Date: 10/30/2020; 4) 1631386/Expiration Date: 05/30/2021; 5) 1631679/Expiration Date: 05/30/2021

Lot Numbers:
Numbers
Product: Lumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure

Lot Numbers/Expiration Dates: 1) 1710206/Expiration Date: 05/30/2022; 2) 1710040/Expiration Date: 01/30/2022; 3) 1610536/Expiration Date: 12/30/2021; 4) 1610423/No Expiration Date; 5) 1610351/No Expiration Date; 6) 1610219/No Expiration Date; 7) 1610090/No Expiration Date

Lot Numbers:
Numbers
Product: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray, Catalog # 986 Product Usage: Surgical procedure

Lot Numbers/Expiration Dates: 1) 1620888/Expiration Date: 12/30/2017 2) 1620367/Expiration Date: 09/01/2017

Lot Numbers:
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 78950
Status: Resolved
Manufacturer: Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables
Manufactured In: United States
Units Affected: 7 products (470 cases; 28 cases; 82 cases; 5 cases; 75 cases; 1037 in total; 15 cases)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.