TIDI Products Recalls Posey Connected Twice-As-Tough Cuffs for Design Defects
TIDI Products is recalling Posey Connected Twice-As-Tough Cuffs because they do not meet design specifications. The recall affects 7,692 units distributed in the US and internationally.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a 'High' severity score (3) when no specific hospitalizations or serious injuries are reported in the source text.
Plain-English summary
TIDI Products is recalling Posey Connected Twice-As-Tough Cuffs, Model # 2796 and Model # 2797, because the products do not meet design specifications. The recall covers 7,692 units, consisting of 7,615 units in the United States and 77 units outside the US.
The affected products were distributed in 32 US states, including Alaska, California, Florida, and Texas, as well as in Canada, France, and the Netherlands. Specific lot numbers for both models are listed in the official recall documentation.
Consumers who have these products should stop using them and contact TIDI Products for further instructions. The FDA has classified this as a Class II recall, indicating a reasonable probability that the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- Posey Connected Twice-As-Tough Cuffs
- Manufacturer
- TIDI PRODUCTS
- Category
- Medical Device — Restraints
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Model # 2796 with Lots #'s : 7109T007
- 7112T001
- 122T083
- 7185T008
- 7192T034
- 7194T051
- 7200T090
- 7250T051
- 7263T007
- 7313T054
- 7355T062
- 7361T073
- 8018T059
- 8038T045
- 8041T035
- 8081T066
- 8122T001
- 8122T088
- 8129T006
- 8130T065
Distribution
Related recalls
Same hazard · design defect
See all →- HighUnited Orthopedic Recalls U2 Total Knee System Femoral Offset Bushings
FDA (Devices) · 2026-08-12
- SevereBioFlo DuraMax catheters recalled as Class I over sheath introducer defect
FDA (Devices) · 2026-04-01
- SevereProGuide chronic dialysis catheters recalled as Class I over sheath introducer defect
FDA (Devices) · 2026-04-01
- SevereDuraMax hemodialysis catheter sheath introducer may not split as intended
FDA (Devices) · 2026-04-01
- SevereMerit 16F splittable sheath introducer recalled as Class I bulk product
FDA (Devices) · 2026-04-01