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FDA (Device enforcement)Recalled 2022-05-25class ii

Mckesson Medical-Surgical Inc. Corporate Office: a. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 3.5ML PLAS VACUTAINER (100/BX), Model Number: 367983. b. BECTON DICKINSON BD Vacutaine

Is my product affected?

a. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 3.5ML PLAS VACUTAINER (100/BX), Model Number: 367983. b. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY8.5ML PLAS VACUTAINER (100/BX Model Number: 367988. c. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP

  • UPC 00382903679836
  • UPC 50382903679831
  • UPC 00382903679881
  • UPC 50382903679886
  • UPC 00382903679867
  • UPC 50382903679862
  • UPC 00382903679874
  • UPC 50382903679879
  • UPC 00382903679812
  • UPC 50382903679817
  • UPC 00382903664306
  • UPC 30382903664307
  • UPC 50382903664301
  • UPC 00382903659784
  • UPC 50382903659789
  • UPC 00382903627615
  • UPC 50382903627610
  • UPC 00382903687749
  • UPC 50382903687744
  • UPC 00382903630837
  • UPC 50382903630832

Check against the official notice below — it lists the full affected range.

What happened

Becton Dickinson BD Vacutainer SST blood collection tubes in 3.5mL plastic versions were recalled due to temperature excursions that occurred at a facility between June and August 2021 before the products were shipped. Exposure to higher temperatures during this period may have affected the product's effectiveness. The recall affects all lots received between June 1, 2021 and September 30, 2021 and was distributed nationwide across multiple lot numbers.

The affected products consist of approximately 684 total boxes across various lot codes. The recall source does not specify a remedy or recommended action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Details from the source

Reason for recall: Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. Distribution: US Nationwide Quantity: a. 67 boxes b. 131 c. 51 d. 121 e. 2 f. 38 g. 16 h. 240 i. 17 j. 41 Lot/code info: GTIN: a. 00382903679836; 50382903679831. b. 00382903679881; 50382903679886. c. 00382903679867; 50382903679862. d. 00382903679874; 50382903679879, e. 00382903679812; 50382903679817. f. 00382903664306; 30382903664307; 50382903664301. g. 00382903659784; 50382903659789. h. 00382903627615; 50382903627610. i. 00382903687749; 50382903687744. j. 00382903630837; 50382903630832.

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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