CLASS II Device recall · Reported 6 Oct 2021 · FDA Enforcement Report

Namic Stopcocks: Namic Stopcock, 200 psi recalled by Medline Industries

Medline Industries is recalling Namic Stopcocks: Namic Stopcock, 200 psi, distributed nationwide in the US. The recall was initiated on 6 Aug 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration dates 12/31/2023-7/12/2024. (1) REF 70015002 - Lot numbers 0000002034, 0000004540, 0000004748, 0000004762, 0000005986, 0000006006, 0000008507, 0000008561, 0000010311, 0000011009, 0000011021, 0000012601, 0000012667, 0000013628, 0000013629, 0000014168, 0000015265, 0000015855, 0000016237, 0000017369; (2) REF 70015003 - Lot numbers 0000002035,0000004399, 0000004781, 0000004859, 0000005958, 0000014171, 0000015997; UPN H965700150031 - Lot number 5658899; (3) REF 70015012 - Lot numbers 0000012075, 0000013640, 0000015290; (4) REF 70015013 - Lot number 0000008503, UPN H965700150131 - Lot numbers 5656213, 5662009; (5) REF 70015015 - Lot numbers 0000005117, 0000007641, 0000007718, 0000011557, 0000014654, 0000017017; UPN H965700150151 - Lot numbers 5655470, 5656214, 5659327; (6) REF 70035002 - Lot numbers 0000002036, 0000002455, 0000008408, 0000008440, 0000008476, 0000010488, 0000015089, 0000017049; UPN H965700350021 - Lot numbers 5654454; 5656220; (7) REF 70035003 - Lot numbers 0000006313, 0000008178, 0000015121; (8) REF 70035008 - Lot numbers 0000003306, 0000010735, 0000014795, 0000016525; UPN H965700350081 - Lot numbers 5653290, 5656221; (9) REF 70035009 - Lot numbers 0000007115, 0000007611, 0000007616, 0000009644, 0000010737, 0000010748, 0000012633, 0000012634, 0000014808, 0000015019, 0000015024, 0000017448; UPN H965700350091 - Lot numbers 5653289, 5658896, 5659333, 5659887, 5659889; (10) REF 70055003 - Lot numbers 0000007025, 0000012635, 0000016518; UPN H965700550031 - Lot numbers 5653288, 5658901, 5662967; (11) REF 70055008 - Lot numbers 0000007081, 0000014807; UPN H965700550081 - Lot numbers 5653287, 5656299; (12) REF 70055009 - Lot numbers 0000003281, 0000003284, 0000007024, 0000007600, 0000007601, 0000009626, 0000009627, 0000010746, 0000012300, 0000012301, 0000012302, 0000014982, 0000015022, 0000016270, 0000016520; UPN H965700550091 - Lot numbers 5653286, 5657315, 5658895, 5658897, 5659900, 5659903, 5659905; and (13) REF 70055017 - Lot numbers 0000007147, 0000010747, 0000015023; UPN H965700550171 - Lot number 5661997.

Quantity recalled816,420 manifolds and stopcocks

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2575-2021
FDA event ID: 88516
Recalling firm: Medline Industries, Northfield, IL
Classification: Class II
Status: Terminated
Recall initiated: 6 Aug 2021
FDA classified: 24 Sep 2021
Reported: 6 Oct 2021
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Device type: Other Medical Devices

Timeline

6 Aug 2021	Recall initiated by company
24 Sep 2021	Classified by FDA	+49 days
6 Oct 2021	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for sterile barrier breach. Microscopic pinholes within the sterile pouch could potentially lead to non-sterile conditions.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

NAMIC Stopcocks: (1) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015002, UPN H965700150021, Three-way Stopcock with Rotating Collar, Rx only, Sterile; (2) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015003, UPN H965700150031, Three-Way Stopcock with Fixed Male Luer Lock, Rx only, Sterile; (3) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015012, UPN H965700150121, Four-way Stopcock with Rotating Collar, Rx only, Sterile; (4) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015013, UPN H965700150131, Four-way Stopcock with Fixed Male Luer Lock, Rx only, Sterile; (5) NAMIC STOPCOCK, 200 psi (14 bar), REF 70015015, UPN H965700150151, One-way Stopcock with Collar, Rx only, Sterile; (6) NAMIC STOPCOCK, 400 psi (28 bar), REF 70035002, UPN H965700350021, Three-way Stopcock with Rotating Collar, Rx only, Sterile; (7) NAMIC STOPCOCK, 400 psi (28 bar), REF 70035003, UPN H965700350031, Three-way Stopcock with Fixed Male Luer Lock, Rx only, Sterile; (8) NAMIC STOPCOCK, 400 psi (28 bar), REF 70035008, UPN H965700350081, Three-way Stopcock with Rotating Adaptor, Rx only, Sterile; (9) NAMIC STOPCOCK, 400 psi (28 bar), REF 70035009, UPN H965700350091, Three-way Stopcock with Rotating Adaptor, Rx only, Sterile; (10) NAMIC STOPCOCK, 1050 psi (72 bar), REF 70055003, UPN H965700550031, Three-way Stopcock with Fixed Male Luer Lock, Rx only, Sterile; (11) NAMIC STOPCOCK, 1050 psi (72 bar), REF 70055008, UPN H965700550081, Three-way Stopcock with Rotating Adapter, Rx only, Sterile; (12) NAMIC STOPCOCK, 1050 psi (72 bar), REF 70055009, UPN H965700550091, Three-way Stopcock with Rotating Adaptor, Rx only, Sterile; and (13) NAMIC STOPCOCK, 1050 psi (72 bar), REF 70055017, UPN H965700550171, One-way Stopcock with Fixed Male Luer Lock, Rx only, Sterile.

Where it was distributed

Worldwide distribution - US Nationwide distribution and the countries of Canada, Australia, Japan, Latvia, Lebanon, Malaysia, Netherlands, Pakistan, People's Republic of China, Panama, Singapore, South Africa, South Korea, Thailand, and United Kingdom.

Nationwide

Questions about this recall

Why was it recalled?

Potential for sterile barrier breach. Microscopic pinholes within the sterile pouch could potentially lead to non-sterile conditions.

Which lots are affected?

Expiration dates 12/31/2023-7/12/2024. (1) REF 70015002 - Lot numbers 0000002034, 0000004540, 0000004748, 0000004762, 0000005986, 0000006006, 0000008507, 0000008561, 0000010311, 0000011009, 0000011021, 0000012601, 0000012667, 0000013628, 0000013629, 0000014168, 0000015265, 0000015855, 0000016237, 0000017369; (2) REF 70015003 - Lot numbers 0000002035,0000004399, 0000004781, 0000004859, 0000005958, 0000014171, 0000015997; UPN H965700150031 - Lot number 5658899; (3) REF 70015012 - Lot numbers 0000012075, 0000013640, 0000015290; (4) REF 70015013 - Lot number 0000008503, UPN H965700150131 - Lot numbers 5656213, 5662009; (5) REF 70015015 - Lot numbers 0000005117, 0000007641, 0000007718, 0000011557, 0000014654, 0000017017; UPN H965700150151 - Lot numbers 5655470, 5656214, 5659327; (6) REF 70035002 - Lot numbers 0000002036, 0000002455, 0000008408, 0000008440, 0000008476, 0000010488, 0000015089, 0000017049; UPN H965700350021 - Lot numbers 5654454; 5656220; (7) REF 70035003 - Lot numbers 0000006313, 0000008178, 0000015121; (8) REF 70035008 - Lot numbers 0000003306, 0000010735, 0000014795, 0000016525; UPN H965700350081 - Lot numbers 5653290, 5656221; (9) REF 70035009 - Lot numbers 0000007115, 0000007611, 0000007616, 0000009644, 0000010737, 0000010748, 0000012633, 0000012634, 0000014808, 0000015019, 0000015024, 0000017448; UPN H965700350091 - Lot numbers 5653289, 5658896, 5659333, 5659887, 5659889; (10) REF 70055003 - Lot numbers 0000007025, 0000012635, 0000016518; UPN H965700550031 - Lot numbers 5653288, 5658901, 5662967; (11) REF 70055008 - Lot numbers 0000007081, 0000014807; UPN H965700550081 - Lot numbers 5653287, 5656299; (12) REF 70055009 - Lot numbers 0000003281, 0000003284, 0000007024, 0000007600, 0000007601, 0000009626, 0000009627, 0000010746, 0000012300, 0000012301, 0000012302, 0000014982, 0000015022, 0000016270, 0000016520; UPN H965700550091 - Lot numbers 5653286, 5657315, 5658895, 5658897, 5659900, 5659903, 5659905; and (13) REF 70055017 - Lot numbers 0000007147, 0000010747, 0000015023; UPN H965700550171 - Lot number 5661997.

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 88516

Reported	Class	Recall	Company	Reason	Where
6 Oct 2021	CLASS II	Namic Manifolds recalled by Medline Industries	Medline Industries	Sterility	Nationwide

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