FDA (Devices) recall action 84688
The FDA (Devices) publishes a recall like this one as 20 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 20 pages.
Product lidstock contains the incorrect expiration date for the product
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
Arrow International Inc. is recalling 180 units of the Arrow EPIDURAL NEEDLE KIT SL-05500 because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,320 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,360 units of the Arrow Epidural Catheterization Kit CK-02220 because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 2,126 units of STIM and INSL CPNB Tuohy needles because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 410 units of Arrow PSI Kits due to incorrect expiration dates on the product lidstock.
Arrow International Inc is recalling 250 units of the Arrow FlexTip Plus Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 205 units of the FlexTip Plus Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling PICC Sets (PR-35052-HPHNM) because the product lidstock contains the incorrect expiration date.
Arrow International is recalling specific lots of PICC kits because the lidstock displays the wrong expiration date.
Arrow International Inc. is recalling 90 units of Arrow SPINAL ANESTHESIA SET ASA-25090-S because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling Arrow Maximal Barrier Drapes because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling Arrow FlexTip Plus Epidural Catheterization Kits because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 140 units of Central Venous Catheterization Kits because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,150 units of FlexTip Plus Combined Spinal Epidural Catheterization Kits because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 540 units of the Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 1,839 units of Arrow Epidural Needle Component AN-05505 because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 160 units of the Arrow Epidural Catheterization Kit (YC-02220) because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 870 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 1,760 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 155 units of the StimuCath Continuous Nerve Block Kit because the product lidstock contains an incorrect expiration date.