Wisconsin recalls
3938 federal recalls on file affecting Wisconsin - 560 Wisconsin-specific plus 3378 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical bile duct exploration kit expiration
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Spectrum catheter tray expiration date
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical extubation set expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical tracheostomy introducer expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck expiration dates on Cook Medical Blue Rhino tracheostomy kits
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical tracheostomy introducer expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical monitoring trays for expiration date
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCOOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical wire guide expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceCookClass IINationwideCheck Cook Medical wire guide expiration dates
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- 2026-04-15FDA-DeviceMolded ProductsClass IINationwideStop using Molded Products MPC-130 Luer caps
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
- 2026-04-15FDA-DeviceBeckman CoulterClass IINationwideStop using Beckman Coulter MicroScan panels
Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
- 2026-04-15FDA-DeviceTornierClass IINationwideCheck Tornier HRS Max shoulder implant parts
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline TAVR Pack kits immediately
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline robotic procedure kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using recalled Medline convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline angiography kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline GLOVE PACK 7.0 medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline medical convenience kits SKU DYNJ86596
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline procedure kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline Special Procedure Tray kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline NAMIC RA syringes immediately
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideNAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107; 6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007; 7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007; 8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107; 9. SY
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline angiographic syringes
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using recalled Medline catheter lab kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline manifold kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideMedline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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