Medical DeviceJun 14, 2017
Beekley Medical 0-SPOT Mammography Skin Markers REF 652 recall — FDA Z-2309-2017
Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels
Class IIIFDA: TerminatedBeekley Corporation
Latest records
Latest recalls — page 1621
The newest recall records with useful source details are listed here.
Medical DeviceJun 14, 2017
Arrow International Arrow(R) Access Kit for use with 4 Fr recall — FDA Z-2288-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Cook Willscher Vas Reapproximator Plate, Surgical Instrument, Supplied sterilized by recall — FDA Z-2312-2017
COOK Medical is initiating a voluntary recall of multiple products because the reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and…
Class IIFDA: TerminatedCook Inc.
Medical DeviceJun 14, 2017
ConvaTec Non-Rebreather Mask, Reservoir Bag, Check Valve, Two Side Valves, No Tubing recall — FDA Z-2234-2017
Non-Rebreather Mask, Reservoir Bag, Check Valve, Two Side Valves, No Tubing, Product Code 226MM
Class IIFDA: TerminatedConvaTec, Inc.
Medical DeviceJun 14, 2017
Arrow VPS Access Kit with Maximal Barrier Precautions for use with 5 Fr recall — FDA Z-2282-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow International Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous recall — FDA Z-2274-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow International Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath recall — FDA Z-2304-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow International Femoral Arterial Line Catheterization Kit The Arrow Arterial recall — FDA Z-2295-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow International QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow recall — FDA Z-2301-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
ConvaTec Oxygen Mask, Standard (Under the Lip) Infant, High Concentration Non-Rebreather, 7 recall — FDA Z-2242-2017
Oxygen Mask, Standard (Under the Lip) Infant, High Concentration Non-Rebreather, 7 ft. (2.1 m) Oxygen Tubing w/FITS-All Oxygen Connector Check Valve, Two Side Valves, Product Code 3266-E
Class IIFDA: TerminatedConvaTec, Inc.
Medical DeviceJun 14, 2017
Arrow PICC with Chlorag+ard Technology A PICC permits venous access to the central recall — FDA Z-2266-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow Access Kit with Maximal Barrier Precautions for use with 5 Fr recall — FDA Z-2289-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow International MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R) recall — FDA Z-2259-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
ConvaTec Oxygen Masks, Elongated (Under Chin) Adult High Conc., Non-Rebreather, 7ft O2 recall — FDA Z-2237-2017
Oxygen Masks, Elongated (Under Chin) Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, One Side Valve, FITS-All Conn., Product Code 3106-E
Class IIFDA: TerminatedConvaTec, Inc.
Medical DeviceJun 14, 2017
Arrow International ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit recall — FDA Z-2270-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2 (HEC200) HEC200 " recall — FDA Z-2316-2017
MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2 (HEC200) control values are outside of specification.
Class IIIFDA: TerminatedMedtest Holdings, Inc.
Medical DeviceJun 14, 2017
Arrow International Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with recall — FDA Z-2277-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Arrow International MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) recall — FDA Z-2253-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Nexstim PLC NBS System 4 (sw version 4.0 or higher), Software update to 4.3.3 and NBS System recall — FDA Z-2320-2017
Software defect: the NBS software may accidentally generate duplicate copies of one or several files.
Class IIFDA: OngoingNexstim PLC
Medical DeviceJun 14, 2017
Arrow International ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit The large-bore recall — FDA Z-2265-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
Acumedia Manufacturers Urea Base Agar, Acumedia PN 7226 Urea Agar Base is used with agar for recall — FDA Z-2221-2017
Storage temperature listed on the label was incorrect. Label stated 2-30¿C. Actual storage temperature is 2-8¿C.
Class IIIFDA: TerminatedAcumedia Manufacturers, Inc.
Medical DeviceJun 14, 2017
Arrow International Pressure Injectable Two-Lumen Central Venous Catheterization Kit with recall — FDA Z-2275-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceJun 14, 2017
ConvaTec Non-Rebreathing Mask, Reservoir Bag, Check Valve, One Side Valve, with Tubing recall — FDA Z-2230-2017
Non-Rebreathing Mask, Reservoir Bag, Check Valve, One Side Valve, with Tubing, Product Code 106-E, Product Code 3226MM, and Product Code 9108MM
Class IIFDA: TerminatedConvaTec, Inc.
Medical DeviceJun 14, 2017
Arrow International Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side recall — FDA Z-2293-2017
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Class IIFDA: TerminatedArrow International 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