A blood collection assembly includes a housing and a cannula extending distally from the housing including a patient end, and a cannula shield removably engaged with a portion of the housing. The cannula shield is capable of shielding at least the patient end of the cannula, and includes a safety shield engagement. The assembly includes a pivoting safety shield engaged with a portion of the housing, which is transitionable from a retracted position in which the patient end of the cannula is exposed, to an extended position in which the patient end of the cannula is shielded by at least a portion of the safety shield. The safety shield includes at least one locking tab releasably engageable with the safety shield engagement, wherein the locking tab is fixedly engageable with a portion of the housing in the extended position.

An automatically locking safety device, e.g., for use in a blood collection procedure, can include a housing, first and second needle covers that are at least partly received in the housing, and a needle that is at least partly received in at least one of the first and second needle covers. The needle can include a proximal tip configured for placement into a patient and a distal tip configured for placement into a blood collection vial. In some embodiments, the first and second needle covers are biased by a biasing member. In some cases, one or both of the first and second needle covers can be locked to prevent axial movement thereof after the blood collection procedure. In certain embodiments, a distal end of the device is configured to connect with a medical connector, such as a needleless IV access device.

A segmented safety cover may include: a) a proximal segment combined with a needle hub; b) a needle cannula that extends from the proximal needle hub to a distal sharpened end; c) a distal end cap with a hollow bore through which the cannula shaft passes; d) a centrally mounted toggle locking mechanism, separating the proximal needle hub from the distal end cap; e) the toggle locking mechanism is torsion spring assisted; f) a proximal cover segment is connected to the hub via a proximal hinge and a distal cover segment is connected to the end cap via a distal hinge; g) said proximal cover segment and said distal cover segment of said toggle locking mechanism being configured with abutting faces when the segmented safety cover is in a safety mode; and h) wherein the proximal hinge, abutting faces and distal hinge are in line in the safe mode.

A medical device is disclosed as having a body comprising an open-ended fluid flow chamber and a laterally offset needle retraction chamber. A frontal attachment that includes a forwardly projecting needle support is slidably coupled to the body. A retractable needle assembly comprising a needle holder, a retraction spring rearwardly biasing the needle holder against the forwardly projecting needle support, and a needle extending forwardly from the forwardly projecting needle support is carried by the frontal attachment, which is laterally slidable with respect to the body from a first position in which the needle is aligned and in fluid communication with the open-ended fluid flow chamber to a second position in which the needle is aligned with the needle retraction chamber to initiate retraction of the needle holder and the needle into the needle retraction chamber.

A needle assembly includes a housing having proximal and distal ends, an IV cannula projecting distally from the housing, and an IV shield having an engagement. The housing has a shield seat and the IV cannula has a distal tip. The IV shield has a pre-use position where the IV shield covers the distal tip of the IV cannula and the engagement is disengaged from the shield seat, and a use position where the engagement is engaged with the shield seat and the IV shield is adapted to move between a non-shielded position, in which the distal tip is exposed, and a shielded position, in which the distal tip is shielded by the IV shield.

An automatically locking safety device, e.g., for use in a blood collection procedure, can include a housing, first and second needle covers that are at least partly received in the housing, and a needle that is at least partly received in at least one of the first and second needle covers. The needle can include a proximal tip configured for placement into a patient and a distal tip configured for placement into a blood collection vial. In some embodiments, the first and second needle covers are biased by a biasing member. In some cases, one or both of the first and second needle covers can be locked to prevent axial movement thereof after the blood collection procedure. In certain embodiments, a distal end of the device is configured to connect with a medical connector, such as a needleless IV access device.

Apparatus and methods for a single, handheld device that provides for both insertion of a catheter and collection of a fluid. Some embodiments further include a needle that assists in the insertion of the catheter into a blood vessel, and which includes a retraction feature that protects the user from an accidental needle stick when the device is ready for disposal. Still further embodiments include a protective cover that prevents a user from accidentally being stuck by a second needle used for the introduction of the patient's blood into a collection device.

A blood collection tube holder having a retractable single needle and a body comprising substantially parallel and laterally spaced apart barrel and needle retraction cavities separated by a partial wall that facilitates lateral movement of the single needle from the barrel cavity into alignment with the needle retraction cavity to initiate needle retraction. The barrel and a frontal attachment to the barrel are cooperatively configured to facilitate relative sliding movement between in a direction that is transverse to the longitudinal axis through the retractable single needle to initiate needle retraction.

A lancing device comprising a housing and a lancet. The lancet comprises a needle and is configured to be movable within the housing from an operational position to a retracted position. The lancing device further comprises a shroud coupled movably to the housing and initially covering the needle, and a biasing member coupled between the lancet and the shroud. The shroud is configured to, when pressed against a sampling site, move rearwards relative to the housing and, at a first point of the rearward movement, allow the needle to contact the sampling site and subsequently, at a second point of the rearward movement, release energy stored in the biasing member to drive the lancet from the operational position to the retracted position. The housing comprises lancet retaining features configured to retain the lancet in the operational position until the shroud reaches the second point of the rearward movement.

An arterial blood module (16) that is removably connectable to an arterial blood collection element (14) is disclosed. The arterial blood module includes a housing (30), a needle (32), a cap (34) removably securable over the needle, a mixing chamber (36), and a safety shield (38) engaged with a portion of the housing and transitionable from a first shield position in which a portion of the needle is exposed to a second shield position in which the needle is shielded by a portion of the safety shield. In one embodiment, the present disclosure includes an arterial blood collection system (10) that includes an arterial blood collection element (14) defining a collection chamber (20) and an arterial blood module (16) removably connectable to a portion of the arterial blood collection element.