Needle Counters; 12.2 x 10.5 x 3.5 cm; 40 Count/70 Capacity; Sterile; Removable Numbered Foam Block; Adhesive Area (Cat. No. 3FA70SSA) Needle Counters; 12.2 x 10.5 x 3.5 cm; 40 Count/70 Capacity; Sterile; Removable Numbered Foam Block; Magnetic Area; (Cat. No. 3FM70SSA) Product Usage: Disposal system for counting of used surgical blades and needles.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog Number: 3FA70SSA Lot Numbers: all lot numbers less than or equal to 843761 Catalog Number: 3FM70SSA Lot Numbers: all lot numbers less than or equal to 933614
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Cardinal Health
- Reason for Recall:
- Small holes (approximately 1 mm or less) found in device unit level packaging potentially compromising product sterility.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Needle Counters; 12.2 x 10.5 x 3.5 cm; 40 Count/70 Capacity; Sterile; Removable Numbered Foam Block; Adhesive Area (Cat. No. 3FA70SSA) Needle Counters; 12.2 x 10.5 x 3.5 cm; 40 Count/70 Capacity; Sterile; Removable Numbered Foam Block; Magnetic Area; (Cat. No. 3FM70SSA) Product Usage: Disposal system for counting of used surgical blades and needles.
Product Codes/Lot Numbers:
Catalog Number: 3FA70SSA Lot Numbers: all lot numbers less than or equal to 843761 Catalog Number: 3FM70SSA Lot Numbers: all lot numbers less than or equal to 933614
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0983-2013
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