Howmedica Osteonics Corp. recalls 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
There is a potential for the outer Tyvek lid to de-bond from the sealed package.
Read the official notice →- Date
- 2022-02-23
- Country
- United States
- Brand
- Howmedica Osteonics
- Product
- 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
- Classification
- Class II
- Units
- Worldwide distribution - US Puerto Rico and the countries of Canada, and…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Howmedica Osteonics recalls
- 2022-06-15
US
Howmedica Osteonics Corp. recalls Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size 5); Catalog…
Stryker has discovered a potential product mix where the size of the Triathlon Tritanium Tibial Component inside the package does not match the package labeling.
FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide in the states of AL, CA, CO, ID, IN,…Official notice →- 2022-04-06
US
Howmedica Osteonics Corp. recalls Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
Potential product mix where the size and/or offset of the Biolox delta Ceramic V40 Femoral Head inside the package does not match the package labeling
FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →- 2022-02-23
US
Howmedica Osteonics Corp. recalls Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
FDA · DeviceHowmedica Osteonics Corp.The product was distributed to the following US states: MIOfficial notice →- 2022-01-12
US
Howmedica Osteonics Corp. recalls Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of…
Triathlon Pro Tibial Preparation Tray may have been kitted with the Triathlon Cemented #1-3 Keel Punch (P/N: 6541-2-013) instead of the Triathlon Pro #0-3 Cemented Keel Punch (P/N: 6541-2-013Y) instrument can lead to…
FDA · DeviceHowmedica Osteonics Corp.US Nationwide distribution in the states of GA, MI, NC, TX.Official notice →- 2021-12-08
US
Howmedica Osteonics Corp. recalls 28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
There is a potential for the outer white Tyvek lid to debond from the sealed package.
US
Other drugs & medical recalls in the United States
- 2022-02-23
US
Merete Medical GmbH recalls Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Incorrect marketing label (25 mm) was applied to product size 20 mm.
US
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Zenition 50, Model #718096
Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used…
FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Domestic distribution to AZ CA FL GA HI IL KS KY MA MD ME MI MN MS NC NE NJ NV…Official notice →US
Oscor Inc. recalls Destino Twist 14F (also branded as Guidestar 14F)
There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.
FDA · DeviceOscor Inc.Distribution to TN and PA in USA OUS distribution to Czech RepublicOfficial notice →US
Envisiontec US Llc recalls FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth
Manufactured in a non-FDA-registered manufacturing facility and product mislabeled as being of German origin
US
Microbiologics Inc recalls KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)
Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating…
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide and the countries of Canada, South…Official notice →US
Hill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
FDA · DeviceHill-Rom, Inc.Worldwide distribution - US Nationwide and the countries of Austria, Austria,…Official notice →