Severity 2 of 5
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Zweigle's Inc. is recalling approximately 6,082 pounds of ready-to-eat olive loaf pork products due to sodium nitrite levels exceeding regulatory limits.
LeMaitre Vascular is recalling AnastoClip GC Closure Systems because the included instructions listed uses not cleared by the FDA.
SPS Sterilization, Inc. is recalling two Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stents because the expiration date on the labeling exceeds the validated shelf life.
Dewey's Bakery is recalling 33,473 bags of Triple Chocolate Brownie Cookies after a customer reported finding mold in the product.
Remel Inc is recalling Remel Thioglycollate Medium (Ref 05152) because products intermittently failed performance testing during stability studies.
Diagnostica Stago is recalling 24,043 kits of STA N¿oplastine¿ CI Plus reagents because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
SPS Sterilization, Inc. is recalling 10 units of resterilized Edwards Lifesciences Aortic Perfusion Cannulas because the expiration date on the labeling exceeds the validated shelf life.
Remel Inc is recalling specific lots of Thioglycollate Medium because the products intermittently failed performance testing during stability studies with anaerobic microorganisms.
Diagnostica Stago is recalling STA N¿oplastine¿ CI in-vitro diagnostic kits because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
SPS Sterilization is recalling 10 units of resterilized venous drainage cannulas because the expiration date on the label exceeds the validated shelf life.
SPS Sterilization is recalling 6 units of Edwards Lifesciences EZ Glide Aortic Cannulas because the expiration date on the label exceeds the validated shelf life.
SPS Sterilization is recalling one unit of an Edwards Lifesciences Femoral Venous Cannula because the expiration date on the label exceeds the validated shelf life.
United Therapeutics is recalling Tyvaso inhalation systems because water can enter the device through the lower water cup sensor.
SPS Sterilization is recalling two units of resterilized Boston Scientific Wallstent RP Endoprosthesis because the labeling expiration date exceeds the validated shelf life.
SPS Sterilization is recalling two Boston Scientific Wallstent tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life of the sterilization process.
SPS Sterilization, Inc. is recalling two units of resterilized Boston Scientific Wallstent Enteral Endoprosthesis because the expiration date on the labeling exceeds the validated shelf life.
Remel Inc is recalling specific lots of Thioglycollate Medium because the products intermittently failed performance testing during stability studies.
SPS Sterilization is recalling two Boston Scientific Wallstent devices because the expiration date on the label exceeds the validated shelf life.
Vascular Technology, Inc. is recalling 10 surgical Doppler transceivers that may be mislabeled as 20 MHz units instead of 8 MHz units.
SPS Sterilization is recalling one unit of an Edwards Lifesciences Femoral Venous Cannula because the expiration date on the label exceeds the validated shelf life.
Micro Therapeutics is recalling 67 units of the ev3 TurboHawk Peripheral Plaque Excision System because packaged accessories are incompatible with the catheter, potentially preventing the removal of excised material.
SPS Sterilization is recalling 5 units of Avid Dual Stage Venous Drainage Cannulas because the expiration date on the label exceeds the validated shelf life.
SPS Sterilization is recalling five units of Edwards Lifesciences venous drainage cannulas because the expiration date on the label exceeds the validated shelf life.
SPS Sterilization, Inc. is recalling three Boston Scientific Wallstent RP Endoprosthesis tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life.
SPS Sterilization is recalling 3 resterilized Venture Rx Catheters because the expiration date on the label exceeds the validated shelf life.