Operating Theatre Medical Supplies List

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Supplier Name
Manufacturer Part No.
Material description
Base Unit of Measure
PFIZER PTY LTD
16050012
DRESSING HSTAT GELFOAM 20X60X7MM
EA
SONY AUSTRALIA LIMITED
UPP-110HG
PAPER THERMOSENSITIVE HIGH GLOSS
EA
KATENA PRODUCTS INC
K7-6750
HANDPIECE MCINTYRE INFUSION
EA
KATENA PRODUCTS INC
K4-8500
SCISSORS STEPHENS STRAIGHT
EA
KATENA PRODUCTS INC
K5-6200
FORCEP BONACCOLTA 1.2MM
EA
KATENA PRODUCTS INC
K20-2054
DELETED – RADIAL VACUUM TREPHINE 7MM
EA
KATENA PRODUCTS INC
K7-6795
HANDLE INFUSION 7.5FR KANSAS KATEENA
EA
KATENA PRODUCTS INC
K3-5523
HOOK IOL KUGLEN KATENA K35523
EA
KATENA PRODUCTS INC
K3-2395
PHACO SPLITTER ROSEN
EA
KATENA PRODUCTS INC
K3-5233
HOOK IOL SINSKEY 2 ANGLE 0.2MM
EA
KATENA PRODUCTS INC
K5-6210
FORCEP CONJUC BONACCOLTO
EA
KATENA PRODUCTS INC
K4-9000
SCISSORS STRAB KNAPP STRAIGHT BLUNT
EA
KATENA PRODUCTS INC
K4-9010
SCISSORS STRAB KNAPP CURVED BLUNT
EA
AESCULAP AG & CO.KG
JG739
LOCK SEAL STERLZ CONT AESCULAP
EA
KARL STORZ GMBH & CO
27502
CONN LUER LOCK WITH STOPCOCK
EA
KARL STORZ GMBH & CO
27068K
KNIFE COLD STRT 2 STEM STORZ
EA
KARL STORZ GMBH & CO
27550A-10
TIP RUBBER WITH HOLE 0.8MM SML
EA
KARL STORZ GMBH & CO
011113-10
ELECTRODE LARGE BALL
EA
KARL STORZ GMBH & CO
011111-10
ELECTRODE KNIFE 24FR
EA
KARL STORZ GMBH & CO
351573W
NEEDLE ZANGER DEBAKERY HEPARIN
EA
KARL STORZ GMBH & CO
351575W
NEEDLE DEBAKERY HEPARIN SMALL
EA
KARL STORZ GMBH & CO
39301A
CONT TELESCOPE 321 X 90 X 45MM
EA
RUSCH INC
121100070
TUBE LARYNGOFLEX 7.0MM ID
EA
STERIS CORPORATION
ST-LCB025
SS1 VERIFY BIOLOGICAL MONITOR KIT
EA
STERIS CORPORATION
ST-S2011
STERILANT SYST 1 STERIS (20)
EA

Bottle Water Recall Over E. Coli

Bottle Water Recall Over E. Coli Affects 11 States, 14 Brands But ‘No Reports Of Any Illness Or Injury’

Jun 22, 2015 10:15 PM By Ed Cara

A voluntary recall of bottled water over E. coli will affect 14 brands across 11 states but likely no risk to the public

Bottled water fans may need to be on alert for a natural ingredient accidentally added to their drink: E. coli.

That’s the warning issued by Niagara Bottling, which has recalled several of its products in the wake of a possible contamination incident. Though the germ, known to occasionally cause diarrhea and nausea, was first detected in a spring water source June 10, the company reports that they weren’t promptly notified in time and has decided to err on the side of caution. They will no longer use that water source as well.

Read more here: click

New Hip Implant Recall Zimmer

New Hip Implant Recall-Zimmer M/L Taper with Kinectiv Technology System
Posted by Richard R. Schlueter
June 23, 2015 1:36 PM

The American Academy of Orthopaedic Surgeons has just issued a Patient Safety Member Alert on the Zimmer M/L Taper with Kinectiv Technology Femoral Stems and Necks. This is a Class 1 Recall per the FDA.

Per the AAOS and the FDA website, The U.S. Food and Drug Administration (FDA) has issued a Class I recall for Zimmer M/L Tapers with Kinectiv Technology Femoral Stems and Necks. The company found a process monitoring failure that led to higher than expected amounts of manufacturing residues left on the devices. These residues can cause serious adverse health issues including allergic reactions, pain, infections, or death. Use of these products may require the need for a revision surgery to replace the affected implant. At this time, the company has not received any complaints related to this issue for any of the lots in distribution.

On May 18, 2015, Zimmer issued recall notification letters with the following instructions for hospital staff, including risk managers and surgeons:

Review the notification and ensure affected personnel are aware of the contents.

Assist your Zimmer sales representative with the quarantine of any affected product.

Your Zimmer sales representative will remove the recalled product from your facility.

The Zimmer M/L Taper with Kinectiv Technology Femoral Stems and Necks are implants used for hip replacements.

Read more here: Legal Examiner