Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215
Terumo Medical
Class I - Dangerous
There is a potential for a loss of package integrity that may compromise the sterility of the product.
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Surgical Instruments
🏥 Medical Devices • 7,015 recalls
3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
Becton Dickinson & Company
Class I - Dangerous
The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 311291155 for epidural or caudal anesthesia
Epimed International
Class I - Dangerous
Mislabeled - The product's labeling contains an incorrect size for the catheter included in the kit. The kit contains a 21 gauge catheter, however the labeling states a 12 gauge catheter is included.
Terumo Needle, 18G x 1", Product Code NN1825R
Terumo Medical
Class I - Dangerous
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Terumo Needle, 30G x 1/2", Product Code NN3013R
Terumo Medical
Class I - Dangerous
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
Terumo Medical
Class I - Dangerous
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220
Terumo Medical
Class I - Dangerous
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Class I - Dangerous
Potential for tube leakage
Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
Cardinal Health 200
Class I - Dangerous
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Zimmer Biomet
Class I - Dangerous
Lack of an adequate sterilization validation.
DeRoyal THE RESOURCE GROUP, CRANI PACK, REF 89-9211.07 custom surgical pack
DeRoyal Industries
Class I - Dangerous
Custom surgical packs are being recalled because it contains Cardinal Health Blunt Cannulas which were recalled due to a manufacturing defect in the cartridge component which could compromise the sterility barrier of the product.
Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509
Zimmer Biomet
Class I - Dangerous
Lack of an adequate sterilization validation.
The device was distributed with the outer carton labeled with the manufacture date and the expiry date reversed. This showed the product as expired before it was manufactured.
The priming volume values printed on the MAHURKA and Argyle acute catheters and Instructions for Use (IFU) are higher than the volumes required to fill each lumen.