Teleflex Recalls
242 recalls on record in the United States
Teleflex Medical Europe Ltd recalls Simplastic Suprapubic Puncture Instruments: Product Code
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
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Teleflex Medical Europe Ltd recalls Rectal Catheters; Product Code Equivalent Code 580114
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
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Teleflex Medical Europe Ltd recalls Latex Rebreathing Bags: Product Code Equivalent Code (a) 1
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
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Teleflex Medical Europe Ltd recalls Baker Jejunostomy Tubes: Product Code Equivalent Code (a
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
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Teleflex Medical recalls Teleflex MEDICAL WECK Visistat 35. Used for the external sk
Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.
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Teleflex Medical recalls Rusch Greenlite MAC 1, Catalog Number 004551001. Used durin
The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.
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Teleflex Medical recalls WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R)
The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.
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Teleflex Medical recalls Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Com
Teleflex is recalling these products because the jaws of the tool tip may break, causing a fragment of the tool tip to fall off during use.
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Teleflex Medical recalls Pilling Knife Handles: a) REF 352950 b) REF 352953 c) R
The knife handles slot depth is out of specification, so blades may not fit on the handles properly.
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Teleflex Medical recalls Percuvance Maryland Dissector Tool Tip The Percutaneous Su
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
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Teleflex Medical recalls Percuvance Gripper Grasper Tool Tip The Percutaneous Surgi
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
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Teleflex Medical recalls Percuvance 29cm Shaft The Percutaneous Surgical System wit
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
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Teleflex Medical recalls Percuvance Johans Grasper Tool Tip The Percutaneous Surgic
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
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Teleflex Medical recalls Percuvance Scissors Tool Tip The Percutaneous Surgical Sys
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
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Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devi
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
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Teleflex Medical recalls Percuvance Clip Applier Tool Tip The Percutaneous Surgical
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
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Teleflex Medical recalls Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are int
Product size listed on the labeling is incorrect.
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Teleflex Medical recalls Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx o
Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.
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Teleflex Medical recalls PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product U
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
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Teleflex Medical recalls PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Pr
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
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Teleflex Medical recalls PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product U
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
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Teleflex Medical recalls INFANT 20/BX, Sterile, Single use Product Usage: Cathete
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Teleflex Medical recalls WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx On
Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device.
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Teleflex Medical recalls Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
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Teleflex Medical recalls Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, C
Labeling error
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Teleflex Medical recalls Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and She
Labeling inconsistency - units labeled with a 7mm tube may contain a size 6.5mm tube, and units labeled 7.5mm tube may contain a size 5.5mm tube.
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TELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
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TELEFLEX LLC recalls Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retr
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
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TELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR STR, REF 243201; retractor
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
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TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasa
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
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Showing 30 of 242 recalls. See all →