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

Mckesson Medical-Surgical Inc. Corporate Office: a. BECTON DICKINSON BD Vacutainer C&S Preservative Urine Tube TUBE, URINE COLL PLAS 4ML (100/BX 10BX/CS), Model Number: BD 364951. b. BECTON DICKINSON

Is my product affected?

a. BECTON DICKINSON BD Vacutainer C&S Preservative Urine Tube TUBE, URINE COLL PLAS 4ML (100/BX 10BX/CS), Model Number: BD 364951. b. BECTON DICKINSON BD Vacutainer C&S Transfer Straw Kit TRANSFER STRAW KIT, URINE 4ML(50/BX 4BX/CS) Model Number: BD 364953. c. BECTON DICKINSON BD Vacutainer COLLECTIO

  • UPC 00382903649518
  • UPC 30382903649519
  • UPC 50382903649513
  • UPC 00382903649532
  • UPC 30382903649533
  • UPC 50382903649537
  • UPC 00382903649570
  • UPC 50382903649575

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

What happened

Mckesson Medical-Surgical Inc. is recalling BD Vacutainer C&S Preservative Urine Collection Tubes (4ML plastic tubes) distributed nationwide. The tubes were exposed to higher temperatures between June and August 2021 at a facility prior to delivery. This temperature exposure may have reduced the product's effectiveness. The recall affects all lots received between June 1, 2021 and September 30, 2021.

The recall record does not specify a remedy or recommended action for consumers who may have affected products.

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. 25 bx b. 53 bx c. 31 cs Lot/code info: GTIN: a. 00382903649518 EA; 30382903649519 PK; 50382903649513. b. 00382903649532; 30382903649533; 50382903649537. c. 00382903649570 EA; 50382903649575 CS

Source

Official record: FDA (Device enforcement) ↗

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

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