Medical Device Technologies, Inc. Angiotech Access Needle. A) Hawkins Blunt Needle. STERILE. Product Number: 216057, 216107, 218057, 218107, 218157. 510k K881957. Qty Dist. - 3,220. B) Winged Guidewire Introducer Needle, Guidewire Introducer Needle, and "WW" Guidewire Introducer Needle. STERILE. Product Number: BGWI1802, BGWI1902, GWI1802, GWI1802WW, GWI1902. GWI1902WW. 510k K974745. Qty Dist: - 51,625. C) Introducer Sheath Needle. STERILE. Product Number: ISN1915. 510k Exempt. Qty Dist: - 1,260. D) Co- Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Angiotech Access Needle. A) Hawkins Blunt Needle. STERILE. Product Number: 216057, 216107, 218057, 218107, 218157. 510k K881957. Qty Dist. - 3,220. B) Winged Guidewire Introducer Needle, Guidewire Introducer Needle, and "WW" Guidewire Introducer Needle. STERILE. Product Number: BGWI1802, BGWI1902, GWI1802, GWI1802WW, GWI1902. GWI1902WW. 510k K974745. Qty Dist: - 51,625. C) Introducer Sheath Needle. STERILE. Product Number: ISN1915. 510k Exempt. Qty Dist: - 1,260. D) Co-
Brand
Medical Device Technologies, Inc.
Lot Codes / Batch Numbers
A) 90851TFD, 91131TZ5, 90571SUT, 91041TT1, 91401UJV, 90821TC4, 90821TC5, 90831TDL, 90961TMO, 91131TZG, 91131U0E, 91331UCU, 90621T0B, 90631T0V, 90761T8P, 90921TKS, 90921TKT, 90961TM0, 91131TY3, 91201U5R, 91271U9U, 91331UCT, 91461UMS, 91821VDN. B) 90471SM2, 90541SRA, 90681T3G, 90751T6V, 91031TS5, 91331UBZ, 90751T79, 90751T7A, 90481SNV, 90541SRC, 90571SUN, 90621SZK, 90771T9K, 90821TCF, 90851TFK, 90901TIR, 90971TOS, 91041TST, 91041TSU, 91271U9B, 91311UAU, 91311UAV, 91311UAW, 91341UEW, 91341UEX, 91531UQI, 91531UQJ, 91621UZ1, 91631UZK, 90471SMB, 90541SS8, 90751T7J, 90841TEF, 90971TO5, 91181U2P, 90781TBC, 90831TE6, 91031TSI, 90851TFF. C) 90551STL, 91381UGK, 91891VI3, 91891VI4, 91891VI5 . D) 90471SMA, 90481SNT, 90481SNW, 90541SS3, 90541SSP, 90551STJ, 90571SUL, 90571SWE, 90611SXU, 90611SYF, 90621SZM, 90631T14, 90681T3U, 90691T4N, 90701T59, 90701T5E, 90701T5K, 90751T6W, 90751T71, 90751T76, 90751T78, 90751T7C, 90751T7I, 90751T7N, 90751T88, 90761T8H, 90761T8L, 90761T8M, 90761T8S, 90771TAS, 90781TB6, 90821TD1, 90831TDR, 90831TE7, 90891TFE, 90891TGQ, 90901TIG, 90901TIH, 90901TIQ, 90921TL2, 90961TM44, 90961TM7, 90971TNE, 90971TO2, 90971TOO, 90971TOQ, 90971TOR, 90981TPS, 90981TQG, 90991TNF, 90991TR1, 90991TR2, 90991TRD, 91031TRZ, 91041TSX, 91041TSY, 91111TWA, 91111TWG, 91131TZ6, 91131TZF, 91131U09, 91131U0G, 91131U0O, 91171U24, 91181TW1, 91181U33, 91181U34, 91181U35, 91191TW4, 91191TW6, 91191U44, 91191U45, 91191U4Q, 91201U5M, 91201U5N, 91271U9N, 91271U9W, 91331UCO, 91341UF4, 91401UIU, 91401UIZ, 91401UJ4, 91401UJA, 91401UJH, 91401UJQ, 91401UJU, 91471UNN, 91481UO8, 91481UOD, 91491UP9, 91531UQK, 91561UUH, 91591UV7, 91631UZI, 91681V2F, 91681V2G, 91681V2H, 91681V2P, 91731V61, 91741V7R, 91761V9C, 91761V9Q, 91801VCB, 91801VCC, 91801VCD, 91801VBM, 90551STY, 90551STZ, 90571SWG, 90611SXI, 90641T15, 90701T5L, 90751T7M, 90751T7P, 90781TBG, 90781TBU, 90851TFI, 90921TL5, 90961TM9, 90971TOT, 90981TQ3, 91041TQ2, 91271U9D, 91271U9E, 91331UC8, 91331UCG, 91331UCS, 91341UEP, 91341UFI, 91561UTV, 91611UYB, 91701V4Q, 91701V4R, 91801VCE.
Products Sold
A) 90851TFD, 91131TZ5, 90571SUT, 91041TT1, 91401UJV, 90821TC4 , 90821TC5, 90831TDL, 90961TMO, 91131TZG , 91131U0E, 91331UCU, 90621T0B, 90631T0V, 90761T8P, 90921TKS, 90921TKT, 90961TM0, 91131TY3, 91201U5R , 91271U9U, 91331UCT, 91461UMS, 91821VDN. B) 90471SM2, 90541SRA, 90681T3G, 90751T6V, 91031TS5, 91331UBZ, 90751T79, 90751T7A, 90481SNV, 90541SRC, 90571SUN, 90621SZK, 90771T9K, 90821TCF, 90851TFK, 90901TIR, 90971TOS, 91041TST, 91041TSU, 91271U9B, 91311UAU, 91311UAV, 91311UAW, 91341UEW, 91341UEX, 91531UQI, 91531UQJ, 91621UZ1, 91631UZK, 90471SMB, 90541SS8, 90751T7J, 90841TEF, 90971TO5, 91181U2P, 90781TBC, 90831TE6, 91031TSI, 90851TFF. C) 90551STL, 91381UGK, 91891VI3, 91891VI4, 91891VI5 . D) 90471SMA, 90481SNT, 90481SNW, 90541SS3, 90541SSP, 90551STJ, 90571SUL, 90571SWE, 90611SXU, 90611SYF, 90621SZM, 90631T14, 90681T3U, 90691T4N, 90701T59, 90701T5E, 90701T5K, 90751T6W, 90751T71, 90751T76, 90751T78, 90751T7C, 90751T7I, 90751T7N, 90751T88, 90761T8H, 90761T8L, 90761T8M, 90761T8S, 90771TAS, 90781TB6, 90821TD1, 90831TDR, 90831TE7, 90891TFE, 90891TGQ, 90901TIG, 90901TIH, 90901TIQ, 90921TL2, 90961TM44, 90961TM7, 90971TNE, 90971TO2, 90971TOO, 90971TOQ, 90971TOR, 90981TPS, 90981TQG, 90991TNF, 90991TR1, 90991TR2, 90991TRD, 91031TRZ, 91041TSX, 91041TSY, 91111TWA, 91111TWG, 91131TZ6, 91131TZF, 91131U09, 91131U0G, 91131U0O, 91171U24, 91181TW1, 91181U33, 91181U34, 91181U35, 91191TW4, 91191TW6, 91191U44, 91191U45, 91191U4Q, 91201U5M, 91201U5N, 91271U9N, 91271U9W, 91331UCO, 91341UF4, 91401UIU, 91401UIZ, 91401UJ4, 91401UJA, 91401UJH, 91401UJQ, 91401UJU, 91471UNN, 91481UO8, 91481UOD, 91491UP9, 91531UQK, 91561UUH, 91591UV7, 91631UZI, 91681V2F, 91681V2G, 91681V2H, 91681V2P, 91731V61, 91741V7R, 91761V9C, 91761V9Q, 91801VCB, 91801VCC, 91801VCD, 91801VBM, 90551STY, 90551STZ, 90571SWG, 90611SXI, 90641T15, 90701T5L, 90751T7M, 90751T7P, 90781TBG, 90781TBU, 90851TFI, 90921TL5, 90961TM9, 90971TOT, 90981TQ3, 91041TQ2, 91271U9D, 91271U9E, 91331UC8, 91331UCG, 91331UCS, 91341UEP, 91341UFI, 91561UTV, 91611UYB, 91701V4Q, 91701V4R, 91801VCE.
Medical Device Technologies, Inc. is recalling Angiotech Access Needle. A) Hawkins Blunt Needle. STERILE. Product Number: 216057, 216107, 21805 due to Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, V. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone Biopsy Needles, Access Needles, Galactography Kit, Stabilization Needles and Needle Guides for packaging integrity.
Recommended Action
Per FDA guidance
Angiotech sent an "URGENT PRODUCT RECALL NOTIFICATION" letter dated September 1, 2009, to all customers. on September 2, 2009 by UPS 2nd day delivery with an assigned tracking number. The letter described the product, problem and action to be taken by customers. The customers were instructed to please review your current inventory and segregate the affected lot numbers, complete the attached Customer Acknowledgement Form and return via fax to our Quality Assurance department at 1-352-338-0662 or 1-800-333-0440. If you are a distributor of this product, you are responsible for notifying any customer you may have sold the product to. If you have any questions concerning this notification, please contact Shannon Brooks at (352) 338-0440 ext.355 or Katrenia Williams at ext. 353.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026