Medical DeviceJun 21, 2017
Medtest Holdings Pointe Scientific Hitachi Total Bilirubin Rl Reagent Product Usage: Two recall — FDA Z-2586-2017
Decrease reactivity of R 1 component.
Class IIFDA: TerminatedMedtest Holdings, Inc.
Latest records
Latest recalls — page 1613
The newest recall records with useful source details are listed here.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N231), REF 413115, 20 cards per recall — FDA Z-2402-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Zimmer Biomet Fem IM Nail 16mmdx42cm, Sterile, Rod, fixation, intramedullary and recall — FDA Z-2552-2017
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Positive Susceptibility card (AST-P633), REF 414994, 20 cards per recall — FDA Z-2464-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Medtronic Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH; Item Number: 8886621933; MAXON recall — FDA Z-2542-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-XN05), REF 413230, 20 cards per recall — FDA Z-2412-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Positive Susceptibility card (AST-P608), REF 22336, 20 cards per recall — FDA Z-2368-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Zimmer Biomet Fem IM Nail 16mmdx44cm, Sterile, Rod, fixation, intramedullary and recall — FDA Z-2554-2017
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-GN65), REF 412608, 20 cards per recall — FDA Z-2385-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-GN77), REF 413434, 20 cards per recall — FDA Z-2426-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N202), REF 412863, 20 cards per recall — FDA Z-2388-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system recall — FDA Z-2194-2017
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Class IIFDA: TerminatedGE Healthcare, LLC
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N253), REF 413722, 20 cards per recall — FDA Z-2434-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Zimmer Biomet Xl por st 25.5x220mm, bowed\, bowed, Sterile, Rod, fixation, intramedullary recall — FDA Z-2583-2017
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-GN49), REF 412091, 20 cards per recall — FDA Z-2380-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Positive Susceptibility card (AST-P597), REF 22298, 20 cards per recall — FDA Z-2360-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Arrow International 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2) recall — FDA Z-2330-2017
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 21, 2017
Merge PACS software recall — FDA Z-2591-2017
When cut lines are shown on an image, the lines may go from being vertical and then shift to horizontal causing confusion to the physician. This may cause a misdiagnosis.
Class IIFDA: TerminatedMerge Healthcare, Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N249), REF 413572, 20 cards per recall — FDA Z-2432-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N228), REF 413145, 20 cards per recall — FDA Z-2406-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N263), REF 413755, 20 cards per recall — FDA Z-2438-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N264), REF 413864, 20 cards per recall — FDA Z-2439-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N314), IVD, REF 417027, 20 cards recall — FDA Z-2478-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
Medical DeviceJun 21, 2017
Biomerieux VITEK 2 Gram Negative Susceptibility card (AST-N334), IVD, REF 418984, 20 cards recall — FDA Z-2498-2017
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Class IIFDA: TerminatedBiomerieux Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026245 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories