Becton Dickinson Infusion Therapy Systems REF: 381923 BD Insyte Autoguard Winged Shielded IV recall — FDA Z-2006-2025
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Complete FDA and NHTSA recall records dated in 2025, organized for browsing by month, category and recalling company.
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Records are ordered by the best available source date.
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Undeclared wheat
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
The recall was the result of the firm's routine sampling program and Listeria monocytogenes was detected in an in-process shrimp sample in a food production environment.
Undeclared Milk.
The quantity of product in each unit does not match the stated weight.
Clostridium botulinum (uneviscerated fish)
Product has Salmonella contamination
Cucumber in salad may be contaminated with Salmonella
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Undeclared Sesame. The firm was notified by a retailer that product labeled as Sea Salt Bagel Crackers contained Everything Bagel Crackers. The Everything Bagel Crackers contains sesame…
Undeclared Milk
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Undeclared wheat
The quantity of product in each unit does not match the stated weight.
Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites
Product has a misbranded Yellow Color. Identified on label at Artificial Yellow Color , and it should be identified as FD&C Yellow #5
Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Discoloration; discolored solution from cracked vials
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.