Tag: particulate_matter

B. Braun Recalls IV Solution Due to Particulate Contamination Risk

20 Aug 2026 4:53 p.m. · Source: US Food and Drug Administration

B. Braun Medical Inc. has voluntarily recalled one lot of Excel® Lactated Ringers Injection, 1000mL, due to particulate matter. The contamination poses risks including pulmonary emboli and organ damage, though no adverse events have been reported.

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B. Braun Medical Recalls Lactated Ringers Injection Over Particulate Matter Risk

20 Aug 2026 8:15 a.m. · Source: US Food and Drug Administration

B. Braun Medical has recalled one lot of Excel Lactated Ringers Injection 1000 mL due to particulate matter, posing risks like pulmonary emboli and organ damage. The product was distributed across the U.S. and Canada.

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Liebel-Flarsheim Recalls OPTIRAY Imaging Vials Over Particulate Contamination

4 Aug 2026 4:22 p.m. · Source: US Food and Drug Administration

Liebel-Flarsheim Company, LLC is recalling OPTIRAY Imaging Bulk Package vials nationwide and in Mexico due to particulate matter. The recall affects hospitals and clinics, posing risks like blood clots, though no adverse events have been reported yet.

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Liebel-Flarsheim Recalls OPTIRAY Imaging Bulk Package Over Particulate Matter Risk

4 Aug 2026 12:48 p.m. · Source: US Food and Drug Administration

Liebel-Flarsheim recalls OPTIRAY Imaging Bulk Package (IBP) 350, 500 mL vials due to particulate matter. The radiographic contrast agent, distributed in the US and Mexico, poses risks of irritation, blood clots, and serious events, though no adverse events are reported.

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American Regent Recalls Papaverine Hydrochloride Injection Due to Particulate Matter

27 Jul 2026 3:53 p.m. · Source: US Food and Drug Administration

American Regent, Inc. has issued a nationwide voluntary recall for a lot of Papaverine Hydrochloride Injection, USP, 60 mg/2 mL. The recall is due to particulate matter, including glass, posing risks like stroke or death, though no adverse events are…

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Baxter Recalls Cefazolin Injection Nationwide Over Cardboard Particulate Matter

27 Jul 2026 3:51 p.m. · Source: US Food and Drug Administration

Baxter International Inc. is recalling Cefazolin in Dextrose Injection nationwide due to cardboard particulate matter. This poses risks like pulmonary emboli and organ damage, though no adverse events are reported yet.

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American Regent Recalls Papaverine Injection Over Particulate Matter Risk

27 Jul 2026 12:58 p.m. · Source: US Food and Drug Administration

American Regent is recalling a lot of Papaverine Hydrochloride Injection due to visible glass and paraformaldehyde particles. This poses serious risks, including stroke and death, though no adverse events are reported yet.

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Baxter Recalls Cefazolin in Dextrose Injection Due to Cardboard Particulates

27 Jul 2026 9:55 a.m. · Source: US Food and Drug Administration

Baxter is recalling a lot of Cefazolin in Dextrose Injection due to cardboard particulate matter found in the solution, posing risks like pulmonary emboli and organ damage.

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Sunny Pharmtech Recalls Cyclophosphamide Injection Over Steel Particulates

24 Jul 2026 2:36 p.m. · Source: US Food and Drug Administration

Sunny Pharmtech is recalling three lots of Cyclophosphamide for Injection, USP, due to steel particulate matter. This poses a risk of serious adverse events, including death, for patients, though no injuries have been reported.

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