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<p>[QUOTE="Anonymous, post: 3265867"]Here's the recall details:</p><p><br /></p><p>AlloSource—Osteocel Plus Cellular Bone Matrix: Donor</p><p>Tested Positive for Hepatitis B Core Antibody</p><p>Product Identifier:</p><p>1 cc Nuvasive Osteocel Plus Cellular Bone Matrix [Consumable]</p><p>Lot Nos.: 091327009, 091327103, 091327104, 091327105, 091327106, 091327107,</p><p>091327108, 091327110, 091327111, 091327112, 091327113, 091327114,</p><p>091327115, 091327116, 091327117, 091327118, 091327119, 091327120,</p><p>091327121, 091327122, 091327123, 091327124, 091327125, 091327126,</p><p>091327127, 091327128, 091327129, 091327130</p><p>Manufacturer: AlloSource [272068], 6278 S Troy Circle, Centennial, CO</p><p>80111-6422, United States</p><p>Problem: FDA states that the above bone matrix was recovered from a donor with a</p><p>positive hepatitis B core antibody serology result. FDA also states the manufacturer</p><p>initiated a recall by telephone call on April 7, 2009. FDA states that the recall is</p><p>complete. No further action is required of customers. The manufacturer has not</p><p>confirmed the information provided in the source material.</p><p>Regulatory Agency: Designation:</p><p>FDA Class II Recall No. B-1694-09, complete[/QUOTE]</p><p><br /></p>
[QUOTE="Anonymous, post: 3265867"]Here's the recall details: AlloSource—Osteocel Plus Cellular Bone Matrix: Donor Tested Positive for Hepatitis B Core Antibody Product Identifier: 1 cc Nuvasive Osteocel Plus Cellular Bone Matrix [Consumable] Lot Nos.: 091327009, 091327103, 091327104, 091327105, 091327106, 091327107, 091327108, 091327110, 091327111, 091327112, 091327113, 091327114, 091327115, 091327116, 091327117, 091327118, 091327119, 091327120, 091327121, 091327122, 091327123, 091327124, 091327125, 091327126, 091327127, 091327128, 091327129, 091327130 Manufacturer: AlloSource [272068], 6278 S Troy Circle, Centennial, CO 80111-6422, United States Problem: FDA states that the above bone matrix was recovered from a donor with a positive hepatitis B core antibody serology result. FDA also states the manufacturer initiated a recall by telephone call on April 7, 2009. FDA states that the recall is complete. No further action is required of customers. The manufacturer has not confirmed the information provided in the source material. Regulatory Agency: Designation: FDA Class II Recall No. B-1694-09, complete[/QUOTE]
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Cafepharma Message Boards | Pharma Sales, Device Sales, Lab Sales
Home
Forums
>
Medical Equipment/Device Sales
>
NuVasive
>
Osteocell Plus vs. Trinity Evolution
>
Cafepharma Message Boards | Pharma Sales, Device Sales, Lab Sales
Home
Forums
>
Medical Equipment/Device Sales
>
NuVasive
>
Osteocell Plus vs. Trinity Evolution
>