Contract manufacturerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list EXP Pharmaceutical Services with 42 device recalls. The most recent is a device recall dated Feb 11, 2015: Medical Device Exchange PT WIRE 300; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OE….
| Feb 11, 2015 | Medical Device Exchange PT WIRE 300; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 38931-04; EXP (repackager), BostonClass II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality s | Device recalls |
| Feb 11, 2015 | Medical Device Exchange 2.15MMX22MM Fluted Spiral Router for CRANI-A; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number A-Class II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality sy | Device recalls |
| Feb 11, 2015 | Medical Device Exchange -Suction Coagulator; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number E2505-10FR; EXP (repackageClass II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality s | Device recalls |
| Feb 11, 2015 | Medical Device Exchange ETS FLEX 45 ENDOSCOPIC ARTICULATING LINEAR CUTTER, 45MM STAPLE; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEClass II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality s | Device recalls |
| Feb 11, 2015 | Medical Device Exchange SECURESTRAP 5mm Absorbable Strap Fixation Device; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog numbeClass II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality sy | Device recalls |
| Feb 11, 2015 | Medical Device Exchange Wire (sternotomy wire); Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 046-072; 046-073; EXP (Class II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality sy | Device recalls |
| Feb 11, 2015 | Medical Device Exchange Round Diamond Bur Extra Coarse; 3.0mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 5820-10-1Class II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality sy | Device recalls |
| Feb 11, 2015 | Medical Device Exchange Insufflation Needle; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number C2201; EXP (repackager), MClass II · EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality s | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
